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Victor Dubowitz

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Co-Publications
Name
50
Muntoni, Francesco
17
Philpot, J
16
Sewry, Caroline
15
Sewry, Caroline
15
Naom, IS
14
Mercuri, Eugenio
12
Dubowitz, Lilly
11
D'Alessandro, M
11
Bobrow, Martin
10
Strong, Peter
9
Davies, Kay
8
Topaloglu, Haluk
8
Scott, Oona
8
Ferlini, Alessandra
7
Pennock, JM

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Publications

TOP 3
Dubowitz V
Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy.
Dubowitz Victor
A short history of the World Muscle Society.
Dubowitz Victor
Prednisone for Duchenne muscular dystrophy.

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All Publications

2006: Dubowitz V
Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy.
Neuromuscular disorders : NMD 2006;16(12):865-6.
2005: Dubowitz Victor
A short history of the World Muscle Society.
Neuromuscular disorders : NMD 2005;15(9-10):642-7.
2005: Dubowitz Victor
Prednisone for Duchenne muscular dystrophy.
Lancet neurology 2005;4(5):264.
2003: Mercuri Eugenio; Brockington Martin; Straub Volker; Quijano-Roy Susana; Yuva Yeliz; Herrmann Ralf; Brown Susan C; Torelli Silvia; Dubowitz Victor; Blake Derek J; Romero Norma B; Estournet Brigitte; Sewry Caroline A; Guicheney Pascale; Voit Thomas; Muntoni Francesco
Phenotypic spectrum associated with mutations in the fukutin-related protein gene.
Annals of neurology 2003;53(4):537-42.
2002: Kinali Maria; Mercuri Eugenio; Main Marion; Muntoni Francesco; Dubowitz Victor
An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy.
Neuromuscular disorders : NMD 2002;12 Suppl 1():S169-74.
2002: Jungbluth H; Müller C R; Halliger-Keller B; Brockington M; Brown S C; Feng L; Chattopadhyay A; Mercuri E; Manzur A Y; Ferreiro A; Laing N G; Davis M R; Roper H P; Dubowitz V; Bydder G; Sewry C A; Muntoni F
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.
Neurology 2002;59(2):284-7.
2002: Dubowitz Victor
Special Centennial Workshop-- 101st ENMC International Workshop: Therapeutic Possibilities in Duchenne Muscular Dystrophy, 30th November-2nd December 2001, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2002;12(4):421-31.
2002: Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
Neuropediatrics 2002;33(1):10-4.
2002: Dubowitz V; Kinali M; Main M; Mercuri E; Muntoni F
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2002;6(3):153-9.
2001: Philpot J; Counsell S; Bydder G; Sewry C A; Dubowitz V; Muntoni F
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?
Neuromuscular disorders : NMD 2001;11(5):489-93.
2001: Skordis L A; Dunckley M G; Burglen L; Campbell L; Talbot K; Patel S; Melki J; Davies K E; Dubowitz V; Muntoni F
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA.
Human genetics 2001;108(4):356-7.
2001: Mercuri E; Rutherford M; De Vile C; Counsell S; Sewry C; Brown S; Bydder G; Dubowitz V; Muntoni F
Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy.
Neuromuscular disorders : NMD 2001;11(3):297-9.
2001: Jungbluth H; Sewry C A; Brown S C; Nowak K J; Laing N G; Wallgren-Pettersson C; Pelin K; Manzur A Y; Mercuri E; Dubowitz V; Muntoni F
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.
Neuromuscular disorders : NMD 2001;11(1):35-40.
2000: Jungbluth H; Sewry C; Brown S C; Manzur A Y; Mercuri E; Bushby K; Rowe P; Johnson M A; Hughes I; Kelsey A; Dubowitz V; Muntoni F
Minicore myopathy in children: a clinical and histopathological study of 19 cases.
Neuromuscular disorders : NMD 2000;10(4-5):264-73.
2000: Brockington M; Sewry C A; Herrmann R; Naom I; Dearlove A; Rhodes M; Topaloglu H; Dubowitz V; Voit T; Muntoni F
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.
American journal of human genetics 2000;66(2):428-35.
2000: Naom I; D'alessandro M; Sewry C A; Jardine P; Ferlini A; Moss T; Dubowitz V; Muntoni F
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy.
Brain : a journal of neurology 2000;123 ( Pt 1)():31-41.
2000: Philpot J; Pennock J; Cowan F; Sewry C A; Dubowitz V; Bydder G; Muntoni F
Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2000;4(3):109-14.
2000: Mercuri E; Goodwin F; Sewry C; Dubowitz V; Muntoni F
Diaphragmatic spinal muscular atrophy with bulbar weakness.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2000;4(2):69-72.
1999: Wallgren-Pettersson C; Pelin K; Hilpelä P; Donner K; Porfirio B; Graziano C; Swoboda K J; Fardeau M; Urtizberea J A; Muntoni F; Sewry C; Dubowitz V; Iannaccone S; Minetti C; Pedemonte M; Seri M; Cusano R; Lammens M; Castagna-Sloane A; Beggs A H; Laing N G; de la Chapelle A
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.
Neuromuscular disorders : NMD 1999;9(8):564-72.
1999: Muntoni F; Goodwin F; Sewry C; Cox P; Cowan F; Airaksinen E; Patel S; Ignatius J; Dubowitz V
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1.
Neuropediatrics 1999;30(5):243-8.
1999: Mercuri E; Gruter-Andrew J; Philpot J; Sewry C; Counsell S; Henderson S; Jensen A; Naom I; Bydder G; Dubowitz V; Muntoni F
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status.
Neuromuscular disorders : NMD 1999;9(6-7):383-7.
1999: D'Alessandro M; Naom I; Ferlini A; Sewry C; Dubowitz V; Muntoni F
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
Human genetics 1999;105(4):308-13.
1999: Philpot J; Bagnall A; King C; Dubowitz V; Muntoni F
Feeding problems in merosin deficient congenital muscular dystrophy.
Archives of disease in childhood 1999;80(6):542-7.
1999: Philpot J; Cowan F; Pennock J; Sewry C; Dubowitz V; Bydder G; Muntoni F
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
Neuromuscular disorders : NMD 1999;9(2):81-5.
1999: Pelin K; Hilpelä P; Donner K; Sewry C; Akkari P A; Wilton S D; Wattanasirichaigoon D; Bang M L; Centner T; Hanefeld F; Odent S; Fardeau M; Urtizberea J A; Muntoni F; Dubowitz V; Beggs A H; Laing N G; Labeit S; de la Chapelle A; Wallgren-Pettersson C
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):2305-10.
1999: Dubowitz V
Forty years of neuromuscular disease: a historical perspective.
Journal of child neurology 1999;14(1):26-8.
1999: Dubowitz V
Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1999;3(2):49-51.
1998: Naom I; D'Alessandro M; Sewry C A; Philpot J; Manzur A Y; Dubowitz V; Muntoni F
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.
Neuromuscular disorders : NMD 1998;8(7):495-501.
1998: Manzur A Y; Sewry C A; Ziprin J; Dubowitz V; Muntoni F
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance.
Neuromuscular disorders : NMD 1998;8(7):467-73.
1998: Taylor J; Sewry C A; Dubowitz V; Muntoni F
Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression.
Neurology 1998;51(4):1116-20.
1998: Campbell L; Daniels R J; Dubowitz V; Davies K E
Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family.
American journal of human genetics 1998;63(1):37-44.
1998: Mercuri E; Anker S; Philpot J; Sewry C; Dubowitz V; Muntoni F
Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy.
Pediatric neurology 1998;18(5):399-401.
1998: Muntoni F; Lichtarowicz-Krynska E J; Sewry C A; Manilal S; Recan D; Llense S; Taylor J; Morris G E; Dubowitz V
Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy.
Neuromuscular disorders : NMD 1998;8(2):72-6.
1998: Muntoni F; Taylor J; Sewry C A; Naom I; Dubowitz V
An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1998;2(1):19-26.
1997: Taylor J; Muntoni F; Dubowitz V; Sewry C A
The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related.
Neuropathology and applied neurobiology 1997;23(5):399-405.
1997: Sewry C A; D'Alessandro M; Wilson L A; Sorokin L M; Naom I; Bruno S; Ferlini A; Dubowitz V; Muntoni F
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.
Neuropediatrics 1997;28(4):217-22.
1997: Campbell L; Potter A; Ignatius J; Dubowitz V; Davies K
Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype.
American journal of human genetics 1997;61(1):40-50.
1997: Taylor J; Muntoni F; Robb S; Dubowitz V; Sewry C
Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?
Neuromuscular disorders : NMD 1997;7(4):211-6.
1997: Naom I; Sewry C; D'Alessandro M; Topaloglu H; Ferlini A; Wilson L; Dubowitz V; Muntoni F
Prenatal diagnosis in merosin-deficient congenital muscular dystrophy.
Neuromuscular disorders : NMD 1997;7(3):176-9.
1997: Sewry C A; Naom I; D'Alessandro M; Sorokin L; Bruno S; Wilson L A; Dubowitz V; Muntoni F
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.
Neuromuscular disorders : NMD 1997;7(3):169-75.
1997: Naom I; D'Alessandro M; Sewry C; Ferlini A; Topaloglu H; Helbling-Leclerc A; Guicheney P; Schwartz K; Akcoren Z; Dubowitz V; Muntoni F
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy.
Human genetics 1997;99(4):535-40.
1997: Tan E; Topaloglu H; Sewry C; Zorlu Y; Naom I; Erdem S; D'Alessandro M; Muntoni F; Dubowitz V
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency.
Neuromuscular disorders : NMD 1997;7(2):85-9.
1997: Naom I S; D'Alessandro M; Topaloglu H; Sewry C; Ferlini A; Helbling-Leclerc A; Guicheney P; Weissenbach J; Schwartz K; Bushby K; Philpot J; Dubowitz V; Muntoni F
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.
Journal of medical genetics 1997;34(2):99-104.
1997: Dubowitz V
Utrophin euphoria.
Neuromuscular disorders : NMD 1997;7(1):5-6.
1997: Topaloglu H; Muntoni F; Dubowitz V; Sewry C
Expression of HLA class I antigens in skeletal muscle is a diagnostic marker in juvenile dermatomyositis.
Journal of child neurology 1997;12(1):60-3.
1997: Goodwin F; Muntoni F; Dubowitz V
Epilepsy in Duchenne and Becker muscular dystrophies.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1997;1(4):115-9.
1996: Mercuri E; Pennock J; Goodwin F; Sewry C; Cowan F; Dubowitz L; Dubowitz V; Muntoni F
Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy.
Neuromuscular disorders : NMD 1996;6(6):425-9.
1996: Dubowitz V
41st ENMC International Workshop on Congenital Muscular Dystrophy 8-10 March 1996, Naarden, The Netherlands.
Neuromuscular disorders : NMD 1996;6(4):295-306.
1996: Sewry C A; Naom I; D'Alessandro M; Ferlini A; Philpot J; Mercuri E; Dubowitz V; Muntoni F
The protein defect in congenital muscular dystrophy.
Biochemical Society transactions 1996;24(2):281S.
1996: Khan Y; Heckmatt J Z; Dubowitz V
Sleep studies and supportive ventilatory treatment in patients with congenital muscle disorders.
Archives of disease in childhood 1996;74(3):195-200.
1996: Sewry C A; Philpot J; Sorokin L M; Wilson L A; Naom I; Goodwin F; D'Alessandro M; Dubowitz V; Muntoni F
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy.
Lancet 1996;347(9001):582-4.
1996: Rodrigues N R; Owen N; Talbot K; Patel S; Muntoni F; Ignatius J; Dubowitz V; Davies K E
Gene deletions in spinal muscular atrophy.
Journal of medical genetics 1996;33(2):93-6.
1995: Helbling-Leclerc A; Topaloglu H; Tomé F M; Sewry C; Gyapay G; Naom I; Muntoni F; Dubowitz V; Barois A; Estournet B
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1995;318(12):1245-52.
1995: Wallgren-Pettersson C; Avela K; Marchand S; Kolehmainen J; Tahvanainen E; Hansen F J; Muntoni F; Dubowitz V; De Visser M; Van Langen I M
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis.
Neuromuscular disorders : NMD 1995;5(6):441-3.
1995: Shorer Z; Philpot J; Muntoni F; Sewry C; Dubowitz V
Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy.
Journal of child neurology 1995;10(6):472-5.
1995: Muntoni F; Wilson L; Marrosu G; Marrosu M G; Cianchetti C; Mestroni L; Ganau A; Dubowitz V; Sewry C
A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
The Journal of clinical investigation 1995;96(2):693-9.
1995: Sewry C A; Philpot J; Mahony D; Wilson L A; Muntoni F; Dubowitz V
Expression of laminin subunits in congenital muscular dystrophy.
Neuromuscular disorders : NMD 1995;5(4):307-16.
1995: Philpot J; Sewry C; Pennock J; Dubowitz V
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle.
Neuromuscular disorders : NMD 1995;5(4):301-5.
1995: Mercuri E; Dubowitz L; Berardinelli A; Pennock J; Jongmans M; Henderson S; Muntoni F; Sewry C; Philpot J; Dubowitz V
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.
Neuropediatrics 1995;26(3):156-62.
1995: Dubowitz V; Fardeau M
Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands.
Neuromuscular disorders : NMD 1995;5(3):253-8.
1995: Philpot J; Topaloglu H; Pennock J; Dubowitz V
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy.
Neuromuscular disorders : NMD 1995;5(3):227-31.
1995: Rapisarda R; Muntoni F; Gobbi P; Dubowitz V
Duchenne muscular dystrophy presenting with failure to thrive.
Archives of disease in childhood 1995;72(5):437-8.
1995: Rodrigues N R; Owen N; Talbot K; Ignatius J; Dubowitz V; Davies K E
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.
Human molecular genetics 1995;4(4):631-4.
1995: Mercuri E; Muntoni F; Berardinelli A; Pennock J; Sewry C; Philpot J; Dubowitz V
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.
Neuropediatrics 1995;26(1):3-7.
1995: Daniels R J; Campbell L; Rodrigues N R; Francis M J; Morrison K E; McLean M; MacKenzie A; Ignatius J; Dubowitz V; Davies K E
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.
Journal of medical genetics 1995;32(2):93-6.
1995: Muntoni F; Melis M A; Ganau A; Dubowitz V
Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.
American journal of human genetics 1995;56(1):151-7.
1995: Philpot J; Muntoni F; Skellett S; Dubowitz V
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: a possible sequel of drug toxicity in first trimester of pregnancy?
Neuromuscular disorders : NMD 1995;5(1):67-9.
1995: Dubowitz V
Chaos in the classification of SMA: a possible resolution.
Neuromuscular disorders : NMD 1995;5(1):3-5.
1995: Dubowitz V; Daniels R J; Davies K E
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q.
Neuromuscular disorders : NMD 1995;5(1):25-9.
1995: Sansome A; Dubowitz V
Intravenous immunoglobulin in juvenile dermatomyositis--four year review of nine cases.
Archives of disease in childhood 1995;72(1):25-8.
1994: Thomas N H; Dubowitz V
The natural history of type I (severe) spinal muscular atrophy.
Neuromuscular disorders : NMD 1994;4(5-6):497-502.
1994: Sewry C A; Matsumura K; Campbell K P; Dubowitz V
Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1994;4(5-6):401-9.
1994: Wilson L A; Cooper B J; Dux L; Dubowitz V; Sewry C A
Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophy.
Neuropathology and applied neurobiology 1994;20(4):359-67.
1994: Eaton D G; Wertheim D; Oozeer R; Dubowitz L M; Dubowitz V
Reversible changes in cerebral activity associated with acidosis in preterm neonates.
Acta paediatrica (Oslo, Norway : 1992) 1994;83(5):486-92.
1994: Quinlivan R M; Robb S A; Hall S M; Honavar M; Hughes R A; Dubowitz V
Infantile axonal neuropathy in two siblings.
Neuromuscular disorders : NMD 1994;4(3):227-32.
1994: Thomas N H; Heckmatt J Z; Rodillo E; Ransley Y F; Dubowitz V
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two cases.
Neuromuscular disorders : NMD 1994;4(2):147-51.
1994: Sewry C A; Sansome A; Matsumura K; Campbell K P; Dubowitz V
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy.
Neuromuscular disorders : NMD 1994;4(2):121-9.
1994: Dubowitz V
22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993.
Neuromuscular disorders : NMD 1994;4(1):75-81.
1994: Wilson L A; Dux L; Cooper B J; Dubowitz V; Sewry C A
Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoforms.
Neuromuscular disorders : NMD 1994;4(1):25-37.
1993: Sherratt T G; Vulliamy T; Dubowitz V; Sewry C A; Strong P N
Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
American journal of human genetics 1993;53(5):1007-15.
1993: Morrison K E; Daniels R J; Suthers G K; Flynn G A; Francis M J; Grewal P K; Dennis C; Buckle V; Ignatius J; Dubowitz V
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).
Human genetics 1993;92(2):133-8.
1993: Sansome A; Royston P; Dubowitz V
Steroids in Duchenne muscular dystrophy; pilot study of a new low-dosage schedule.
Neuromuscular disorders : NMD 1993;3(5-6):567-9.
1993: Clerk A; Morris G E; Dubowitz V; Davies K E; Sewry C A
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle.
The Histochemical journal 1993;25(8):554-61.
1993: Sewry C A; Sansome A; Clerk A; Sherratt T G; Hasson N; Rodillo E; Heckmatt J Z; Strong P N; Dubowitz V
Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.
Neuromuscular disorders : NMD 1993;3(2):141-8.
1993: Dux L; Cooper B J; Sewry C A; Dubowitz V
Notechis scutatus venom increases the yield of proliferating muscle cells from biopsies of normal and dystrophic canine muscle--a possible source for myoblast transfer studies.
Neuromuscular disorders : NMD 1993;3(1):23-9.
1992: Gangopadhyay S B; Sherratt T G; Heckmatt J Z; Dubowitz V; Miller G; Shokeir M; Ray P N; Strong P N; Worton R G
Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
American journal of human genetics 1992;51(3):562-70.
1992: Clerk A; Sewry C A; Dubowitz V; Strong P N
Characterisation of dystrophin in fetuses at risk for Duchenne muscular dystrophy.
Journal of the neurological sciences 1992;111(1):82-91.
1992: Dubowitz V
The muscular dystrophies.
Postgraduate medical journal 1992;68(801):500-6.
1992: Hamill G; Saunders C; Heckmatt J; Dubowitz V; Stanhope R
"Catch-up" growth in steroid dependent dermatomyositis treated with cyclosporin-A.
The European journal of medicine 1992;1(1):16-8.
1992: Daniels R J; Suthers G K; Morrison K E; Thomas N H; Francis M J; Mathew C G; Loughlin S; Heiberg A; Wood D; Dubowitz V
Prenatal prediction of spinal muscular atrophy.
Journal of medical genetics 1992;29(3):165-70.
1992: Eaton D G; Wertheim D; Oozeer R; Royston P; Dubowitz L; Dubowitz V
The effect of pethidine on the neonatal EEG.
Developmental medicine and child neurology 1992;34(2):155-63.
1992: Daniels R J; Thomas N H; MacKinnon R N; Lehner T; Ott J; Flint T J; Dubowitz V; Ignatius J; Donner M; Zerres K
Linkage analysis of spinal muscular atrophy.
Genomics 1992;12(2):335-9.
1992: Cole C G; Abbs S J; Dubowitz V; Hodgson S V; Warner J; Merlini L; Bobrow M
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII.
Neuromuscular disorders : NMD 1992;2(1):51-7.
1992: Hodgson S V; Abbs S; Clark S; Manzur A; Heckmatt J Z; Dubowitz V; Bobrow M
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability.
Neuromuscular disorders : NMD 1992;2(4):269-76.
1992: Quinlivan R M; Dubowitz V
Cardiac transplantation in Becker muscular dystrophy.
Neuromuscular disorders : NMD 1992;2(3):165-7.
1992: Manzur A Y; Hyde S A; Rodillo E; Heckmatt J Z; Bentley G; Dubowitz V
A randomized controlled trial of early surgery in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1992;2(5-6):379-87.
1992: Sewry C A; Wilson L A; Dux L; Dubowitz V; Cooper B J
Experimental regeneration in canine muscular dystrophy--1. Immunocytochemical evaluation of dystrophin and beta-spectrin expression.
Neuromuscular disorders : NMD 1992;2(5-6):331-42.
1991: Wertheim D F; Murdoch Eaton D G; Oozeer R C; Connell J A; Dubowitz L M; Dubowitz V; Willetts R; Wootton R
A new system for cotside display and analysis of the preterm neonatal electroencephalogram.
Developmental medicine and child neurology 1991;33(12):1080-6.
1991: Peters A M; Heckmatt J Z; Hasson N; Henderson B L; el-Meleigy D; Rose M L; Dubowitz V
Renal haemodynamics of cyclosporin A nephrotoxicity in children with juvenile dermatomyositis.
Clinical science (London, England : 1979) 1991;81(2):153-9.
1991: Clerk A; Rodillo E; Heckmatt J Z; Dubowitz V; Strong P N; Sewry C A
Characterisation of dystrophin in carriers of Duchenne muscular dystrophy.
Journal of the neurological sciences 1991;102(2):197-205.
1991: Dubowitz V
Recent advances in neuromuscular disorders in childhood.
Acta paediatrica Japonica; Overseas edition 1991;33(2):198-205.
1991: Bush A; Dubowitz V
Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy.
Neuromuscular disorders : NMD 1991;1(3):201-4.
1991: Davies K E; Thomas N H; Daniels R J; Dubowitz V
Molecular studies of spinal muscular atrophy.
Neuromuscular disorders : NMD 1991;1(2):83-5.
1991: Sewry C A; Clerk A; Heckmatt J Z; Vyse T; Dubowitz V; Strong P N
Dystrophin abnormalities in polymyositis and dermatomyositis.
Neuromuscular disorders : NMD 1991;1(5):333-9.
1990: McDouall R M; Dunn M J; Dubowitz V
Nature of the mononuclear infiltrate and the mechanism of muscle damage in juvenile dermatomyositis and Duchenne muscular dystrophy.
Journal of the neurological sciences 1990;99(2-3):199-217.
1990: Heckmatt J Z; Loh L; Dubowitz V
Night-time nasal ventilation in neuromuscular disease.
Lancet 1990;335(8689):579-82.
1990: Scott O M; Hyde S A; Vrbová G; Dubowitz V
Therapeutic possibilities of chronic low frequency electrical stimulation in children with Duchenne muscular dystrophy.
Journal of the neurological sciences 1990;95(2):171-82.
1989: Hodgson S; Hart K; Abbs S; Heckmatt J; Rodillo E; Bobrow M; Dubowitz V
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.
Journal of medical genetics 1989;26(11):682-93.
1989: Dubowitz V
The Duchenne dystrophy story: from phenotype to gene and potential treatment.
Journal of child neurology 1989;4(4):240-50.
1989: Heckmatt J; Rodillo E; Dubowitz V
Management of children: pharmacological and physical.
British medical bulletin 1989;45(3):788-801.
1989: Rodillo E; Noble-Jamieson C M; Aber V; Heckmatt J Z; Muntoni F; Dubowitz V
Respiratory muscle training in Duchenne muscular dystrophy.
Archives of disease in childhood 1989;64(5):736-8.
1989: Heckmatt J; Hasson N; Saunders C; Thompson N; Peters A M; Cambridge G; Rose M; Hyde S A; Dubowitz V
Cyclosporin in juvenile dermatomyositis.
Lancet 1989;1(8646):1063-6.
1989: Rodillo E; Marini M L; Heckmatt J Z; Dubowitz V
Scoliosis in spinal muscular atrophy: review of 63 cases.
Journal of child neurology 1989;4(2):118-23.
1989: Connell J; Oozeer R; de Vries L; Dubowitz L M; Dubowitz V
Clinical and EEG response to anticonvulsants in neonatal seizures.
Archives of disease in childhood 1989;64(4 Spec No):459-64.
1989: Connell J; Oozeer R; de Vries L; Dubowitz L M; Dubowitz V
Continuous EEG monitoring of neonatal seizures: diagnostic and prognostic considerations.
Archives of disease in childhood 1989;64(4 Spec No):452-8.
1989: Rutherford M A; Heckmatt J Z; Dubowitz V
Congenital myotonic dystrophy: respiratory function at birth determines survival.
Archives of disease in childhood 1989;64(2):191-5.
1989: McDouall R M; Dunn M J; Dubowitz V
Expression of class I and class II MHC antigens in neuromuscular diseases.
Journal of the neurological sciences 1989;89(2-3):213-26.
1989: Heckmatt J Z; Loh L; Dubowitz V
Nocturnal hypoventilation in children with nonprogressive neuromuscular disease.
Pediatrics 1989;83(2):250-5.
1989: Voit T; Patel K; Dunn M J; Dubowitz V; Strong P N
Distribution of dystrophin, nebulin and Ricinus communis I (RCA-I)-binding glycoprotein in tissues of normal and mdx mice.
Journal of the neurological sciences 1989;89(2-3):199-211.
1989: Lary S; De Vries L S; Kaiser A; Dubowitz L M; Dubowitz V
Auditory brain stem responses in infants with posthaemorrhagic ventricular dilatation.
Archives of disease in childhood 1989;64(1 Spec No):17-23.
1989: Voit T; Patel K; Sewry C A; Strong P N; Dubowitz V; Dunn M J
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft für Kinderheilkunde 1989;137(1):20-7.
1989: Patel K; Leevers S; Abbs S; Hart K A; Heckmatt J Z; Bobrow M; Dubowitz V
Absence of dystrophin in Becker muscular dystrophy.
Lancet 1989;1(8628):47.
1989: Cambridge G; Faith A; Saunders C; Dubowitz V
A comparative study of in vitro proliferative responses to mitogens and immunoglobulin production in patients with inflammatory muscle disease.
Clinical and experimental rheumatology 1989;7(1):27-33.
1988: Barrett R; Hyde S A; Scott O M; Dubowitz V
Changes in center of gravity in boys with Duchenne muscular dystrophy.
Muscle & nerve 1988;11(11):1157-63.
1988: Patel K; Voit T; Dunn M J; Strong P N; Dubowitz V
Dystrophin and nebulin in the muscular dystrophies.
Journal of the neurological sciences 1988;87(2-3):315-26.
1988: Rodillo E B; Fernandez-Bermejo E; Heckmatt J Z; Dubowitz V
Prevention of rapidly progressive scoliosis in Duchenne muscular dystrophy by prolongation of walking with orthoses.
Journal of child neurology 1988;3(4):269-74.
1988: Connell J; de Vries L; Oozeer R; Regev R; Dubowitz L M; Dubowitz V
Predictive value of early continuous electroencephalogram monitoring in ventilated preterm infants with intraventricular hemorrhage.
Pediatrics 1988;82(3):337-43.
1988: Heckmatt J Z; Hyde S A; Gabain A; Dubowitz V
Therapeutic trial of isaxonine in Duchenne muscular dystrophy.
Muscle & nerve 1988;11(8):836-47.
1988: Patel K; Strong P N; Dubowitz V; Dunn M J
Calmodulin-binding profiles for nebulin and dystrophin in human skeletal muscle.
FEBS letters 1988;234(2):267-71.
1988: Robb S A; Fielder A H; Saunders C E; Davey N J; Burley M W; Lord D H; Batchelor J R; Dubowitz V
C4 complement allotypes in juvenile dermatomyositis.
Human immunology 1988;22(1):31-8.
1988: Voit T; Sewry C A; Dunn M J; Dubowitz V
Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus.
Journal of the neurological sciences 1988;84(2-3):301-14.
1988: Heckmatt J Z; Pier N; Dubowitz V
Assessment of quadriceps femoris muscle atrophy and hypertrophy in neuromuscular disease in children.
Journal of clinical ultrasound : JCU 1988;16(3):177-81.
1988: Heckmatt J Z; Pier N; Dubowitz V
Measurement of quadriceps muscle thickness and subcutaneous tissue thickness in normal children by real-time ultrasound imaging.
Journal of clinical ultrasound : JCU 1988;16(3):171-6.
1988: Heckmatt J Z; Pier N; Dubowitz V
Real-time ultrasound imaging of muscles.
Muscle & nerve 1988;11(1):56-65.
1988: Dubowitz V
Responses of diseased muscle to electrical and mechanical intervention.
Ciba Foundation symposium 1988;138():240-55.
1987: Sewry C A; Dubowitz V; Abraha A; Luzio J P; Campbell A K
Immunocytochemical localisation of complement components C8 and C9 in human diseased muscle. The role of complement in muscle fibre damage.
Journal of the neurological sciences 1987;81(2-3):141-53.
1987: Connell J; Oozeer R; Regev R; De Vries L S; Dubowitz L M; Dubowitz V
Continuous four-channel EEG monitoring in the evaluation of echodense ultrasound lesions and cystic leucomalacia.
Archives of disease in childhood 1987;62(10):1019-24.
1987: Connell J A; Oozeer R; Dubowitz V
Continuous 4-channel EEG monitoring: a guide to interpretation, with normal values, in preterm infants.
Neuropediatrics 1987;18(3):138-45.
1987: De Vries L S; Connell J A; Dubowitz L M; Oozeer R C; Dubowitz V; Pennock J M
Neurological, electrophysiological and MRI abnormalities in infants with extensive cystic leukomalacia.
Neuropediatrics 1987;18(2):61-6.
1987: Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
Journal of medical genetics 1987;24(3):152-9.
1987: Hart K A; Hodgson S; Walker A; Cole C G; Johnson L; Dubowitz V; Bobrow M
DNA deletions in mild and severe Becker muscular dystrophy.
Human genetics 1987;75(3):281-5.
1986: Hart K; Cole C; Walker A; Hodgson S; Johnson L; Dubowitz V; Ray P; Worton R; Bobrow M
The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.
Journal of medical genetics 1986;23(6):516-20.
1986: Scott O M; Vrbová G; Hyde S A; Dubowitz V
Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulation.
Journal of neurology, neurosurgery, and psychiatry 1986;49(12):1427-34.
1986: Hodgson S; Boswinkel E; Cole C; Walker A; Dubowitz V; Granata C; Merlini L; Bobrow M
A linkage study of Emery-Dreifuss muscular dystrophy.
Human genetics 1986;74(4):409-16.
1986: Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
Linkage studies in Duchenne and Becker muscular dystrophies.
Journal of medical genetics 1986;23(6):538-47.
1986: Kunkel L M; Hejtmancik J F; Caskey C T; Speer A; Monaco A P; Middlesworth W; Colletti C A; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt S A; Bartlett R; Pericak-Vance M A; Roses A D; Thompson M W; Ray P N; Worton R G; Fischbeck K H; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan J C; Emery A; Dorkins H; McGlade S; Davies K E; Boehm C; Arveiler B; Lemaire C; Morgan G J; Denton M J; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox D E; Affara N A; Ferguson-Smith M A; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen G J; Pearson P L; Greenberg C R; Hamerton J L; Wrogemann K; Doherty R A; Polakowska R; Hyser C; Quirk S; Thomas N; Harper J F; Darras B T; Francke U
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: Hodgson S; Hart K; Walker A; Cole C; Johnson L; Bobrow M; Dubowitz V; Kunkel L
DNA deletion in boy with Becker muscular dystrophy.
Lancet 1986;1(8486):918.
1986: Noble-Jamieson C M; Heckmatt J Z; Dubowitz V; Silverman M
Effects of posture and spinal bracing on respiratory function in neuromuscular disease.
Archives of disease in childhood 1986;61(2):178-81.
1985: Lary S; Briassoulis G; de Vries L; Dubowitz L M; Dubowitz V
Hearing threshold in preterm and term infants by auditory brainstem response.
The Journal of pediatrics 1985;107(4):593-9.
1985: Scott O M; Vrbová G; Hyde S A; Dubowitz V
Effects of chronic low frequency electrical stimulation on normal human tibialis anterior muscle.
Journal of neurology, neurosurgery, and psychiatry 1985;48(8):774-81.
1985: de Vries L S; Dubowitz L M; Dubowitz V; Kaiser A; Lary S; Silverman M; Whitelaw A; Wigglesworth J S
Predictive value of cranial ultrasound in the newborn baby: a reappraisal.
Lancet 1985;2(8447):137-40.
1985: Heckmatt J Z; Dubowitz V; Hyde S A; Florence J; Gabain A C; Thompson N
Prolongation of walking in Duchenne muscular dystrophy with lightweight orthoses: review of 57 cases.
Developmental medicine and child neurology 1985;27(2):149-54.
1982: Hyde S A; Scott O M; Goddard C M; Dubowitz V
Prolongation of ambulation in Duchenne muscular dystrophy by appropriate orthoses.
Physiotherapy 1982;68(4):105-8.
1982: Scott O M; Hyde S A; Goddard C; Dubowitz V
Quantitation of muscle function in children: a prospective study in Duchenne muscular dystrophy.
Muscle & nerve 1982;5(4):291-301.
1981: Scott O M; Hyde S A; Goddard C; Dubowitz V
Prevention of deformity in Duchenne muscular dystrophy. A prospective study of passive stretching and splintage.
Physiotherapy 1981;67(6):177-80.
1981: Scott O M; Hyde S A; Goddard C; Jones R; Dubowitz V
Effect of exercise in Duchenne muscular dystrophy.
Physiotherapy 1981;67(6):174-6.

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