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Gösta Holmgren

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Gösta Holmgren; Urban Hellman; Hans-Eric Lundgren; Ola Sandgren; Ole B Suhr
Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.
Gösta Holmgren; Urban Hellman; Jenni Jonasson; Hans-Eric Lundgren; Per Westermark; Ole B Suhr
A Swedish family with the rare Phe33Leu transthyretin mutation.
Gösta Holmgren; Urban Hellman; Intissar Anan; Hans-Eric Lundgren; Jenni Jonasson; Christina Stafberg; Sämi Fahoum; Ole B Suhr
Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.

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2005: Gösta Holmgren; Urban Hellman; Hans-Eric Lundgren; Ola Sandgren; Ole B Suhr
Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.
Journal of medical genetics 2005;42(12):953-6.
2005: Gösta Holmgren; Urban Hellman; Jenni Jonasson; Hans-Eric Lundgren; Per Westermark; Ole B Suhr
A Swedish family with the rare Phe33Leu transthyretin mutation.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2005;12(3):189-92.
2005: Gösta Holmgren; Urban Hellman; Intissar Anan; Hans-Eric Lundgren; Jenni Jonasson; Christina Stafberg; Sämi Fahoum; Ole B Suhr
Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2005;12(3):184-8.
2005: Uwe Fuchs; Armin Zittermann; Ole Suhr; Gösta Holmgren; Gero Tenderich; Kazutomo Minami; Reiner Koerfer
Heart transplantation in a 68-year-old patient with senile systemic amyloidosis.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2005;5(5):1159-62.
2004: Ole B Suhr; Gösta Holmgren; Erik Lundgren
Gene therapy: lessons learned from liver transplantation for transthyretin-amyloidosis.
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 2004;10(12):1551-3.
2004: Gösta Holmgren; Lars Wikström; Hans-Eric Lundgren; Ole B Suhr
Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins.
Journal of internal medicine 2004;256(5):453-6.
2004: Gösta Holmgren; Hans-Eric Lundgren; Ole B Suhr
Successful pregnancies and fatherhood in familial amyloidotic polyneuropathy (FAP Val30Met) patients with liver transplantation.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2004;11(2):125-9.
2004: Elisabet Einarsdottir; Anna Carlsson; Jan Kare Minde; Göran Toolanen; Olle Svensson; Göran Solders; Gösta Holmgren; Dan Holmberg; Monica Holmberg
A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception.
Human molecular genetics 2004;13(8):799-805.
2003: Ole B Suhr; I Hastrup Svendsen; R Andersson; A Danielsson; Gösta Holmgren; PJ Ranløv
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
Journal of internal medicine 2003;254(3):225-35.
2003: Erik Forestier; Sverre Heim; Elisabeth Blennow; Georg Borgström; Gösta Holmgren; Kristina Heinonen; Johann H Johannsson; Gitte B Kerndrup; Mette K Andersen; Catarina Lundin; Ann Nordgren; Richard Rosenquist; Birgitta Swolin; Bertil Johansson
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
British journal of haematology 2003;121(4):566-77.
2003: Irina Golovleva; Sanjoy K Bhattacharya; Zhiping Wu; Natacha Shaw; Yanwu Yang; Khurshid Andrabi; Karen A West; Marie S I Burstedt; Kristina Forsman; Gösta Holmgren; Ola Sandgren; Noa Noy; Jun Qin; John W Crabb
Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions.
The Journal of biological chemistry 2003;278(14):12397-402.
2003: Elisabet Einarsdottir; Ingegerd Söderström; Anna Löfgren-Burström; Susann Haraldsson; Sofie Nilsson-Ardnor; Carlos Penha-Goncalves; Lisbet Lind; Gösta Holmgren; Monica Holmberg; Kjell Asplund; Dan Holmberg
The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease.
European journal of human genetics : EJHG 2003;11(1):81-4.
2002: A Carlsson; Lars Forsgren; Per-Olof Nylander; U Hellman; Kristina Forsman-Semb; Gösta Holmgren; D Holmberg; M Holmberg
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.
Neurology 2002;59(11):1804-7.
2002: Carina K Mårdh; Birgitta Bäckman; Gösta Holmgren; Jan C C Hu; James P Simmer; Kristina Forsman-Semb
A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
Human molecular genetics 2002;11(9):1069-74.
2002: Irina Golovleva; Johan Hultdin; Göran Roos; Ake Wahlin; Gösta Holmgren
Co-existence of pseudo-Chediak-Higashi anomaly and double minutes containing C-MYC oncogene in three patients with AML M2.
Leukemia 2002;16(1):152-4.
2001: C Sun; Lisbeth Tranebjaerg; Torberg Torbergsen; Gösta Holmgren; Marijke Van Ghelue
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia.
European journal of human genetics : EJHG 2001;9(12):903-9.
2001: Ann Nordgren; Filip Farnebo; B Johansson; Gösta Holmgren; Erik Forestier; Catharina Larsson; Stefan Söderhäll; Magnus Nordenskjöld; Elisabeth Blennow
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.
European journal of haematology 2001;66(5):297-304.
2001: Carina K Mårdh; Birgitta Bäckman; Darrin Simmons; Irina Golovleva; Ting Ting Gu; Gösta Holmgren; Mary MacDougall; Kristina Forsman-Semb
Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.
European journal of oral sciences 2001;109(1):8-13.
2001: Ole B Suhr; K Lång; Lars Wikström; Intissar Anan; Yukio Ando; Magdy El-Salhy; Gösta Holmgren; K Tashima
Scavenger treatment of free radical injury in familial amyloidotic polyneuropathy: a study on Swedish transplanted and non-transplanted patients.
Scandinavian journal of clinical and laboratory investigation 2001;61(1):11-8.
2000: Jenni Jonasson; Vesa Juvonen; Pertti Sistonen; Jaakko Ignatius; D Johansson; E J Björck; J Wahlström; A Melberg; Gösta Holmgren; Lars Forsgren; Monica Holmberg
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
European journal of human genetics : EJHG 2000;8(12):918-22.
2000: Marijke Van Ghelue; H L Eriksen; Vesna Ponjavic; Toril Fagerheim; Sten Andréasson; Kristina Forsman-Semb; Ola Sandgren; Gösta Holmgren; Lisbeth Tranebjaerg
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
Ophthalmic genetics 2000;21(4):197-209.
2000: Christine Klein; Karla Schilling; Rachel Saunders-Pullman; Jennifer Garrels; Xandra O Breakefield; Mitchell F Brin; D DeLeon; Dana Doheny; Stanley Fahn; J S Fink; Lars Forsgren; Jennifer Friedman; S Frucht; Juliette Harris; Gösta Holmgren; Bernhard Kis; Roger Kurlan; M Kyllerman; Anthony E Lang; Joanne Leung; Deborah Raymond; J D Robishaw; G Sanner; Eberhard Schwinger; Rowena Tabamo; Michele Tagliati
A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.
American journal of human genetics 2000;67(5):1314-9.
2000: Bo-Göran Ericzon; Gösta Holmgren; E Lundgren; Ole B Suhr
New structural information and update on liver transplantation in transthyretin-associated amyloidosis. Report from the 4th International Symposium on Familial Amyloidotic Polyneuropathy and Other Transthyretin Related Disorders & the 3rd International Workshop on Liver Transplantation in Familial Amyloid Polyneuropathy, Umeå Sweden, June 1999.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2000;7(2):145-7.
2000: T Janunger; Intissar Anan; Gösta Holmgren; O Lövheim; Per-Ingvar Ohlsson; Ole B Suhr; K Tashima
Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2000;7(2):137-40.
2000: C Mambule; Yukio Ando; Intissar Anan; Gösta Holmgren; Ola Sandgren; T Stigbrandt; K Tashima; Ole B Suhr
Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol.
Biochimica et biophysica acta 2000;1474(3):331-6.
2000: Christine Klein; Nadia Gurvich; Miguel Sena-Esteves; Susan Bressman; Mitchell F Brin; Barbara J Ebersole; S Fink; Lars Forsgren; Jennifer Friedman; D Grimes; Gösta Holmgren; M Kyllerman; Anthony E Lang; Deborah de Leon; Joanne Leung; C Prioleau; Deborah Raymond; G Sanner; Rachel Saunders-Pullman; Peter Vieregge; J Wahlström; Xandra O Breakefield; Patricia L Kramer; Laurie J Ozelius; Stuart C Sealfon
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.
Annals of neurology 2000;47(3):369-73.
1999: Javier C Lendoire; Pedro Trigo; HF Aziz; María C Romero; O Inventarza; Yukio Ando; K Tashima; Per-Ingvar Ohlsson; K Cederquist; Gösta Holmgren; Ole B Suhr
Variant transthyretin (TTR) amyloidosis in Argentina. Detection of the trait by electrospray ionization mass spectrometry of lyophilized TTR immunoprecipitate.
Scandinavian journal of clinical and laboratory investigation 1999;59(8):613-8.
1999: K Tashima; Ole B Suhr; Yukio Ando; Gösta Holmgren; Takeshi Yamashita; Konen Obayashi; Hisayasu Terazaki; Makoto Uchino
Gastrointestinal dysfunction in familial amyloidotic polyneuropathy (ATTR Val30Met)--comparison of Swedish and Japanese patients.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 1999;6(2):124-9.
1999: Marie S I Burstedt; Ola Sandgren; Gösta Holmgren; Kristina Forsman-Semb
Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.
Investigative ophthalmology & visual science 1999;40(5):995-1000.
1999: Jens Johansson; Gösta Holmgren; Lars Forsgren; M Holmberg
[Growing genes cause neurological diseases].
Läkartidningen 1999;96(8):897-900.
1998: O B Suhr; Gösta Holmgren; Y Ando
Improvement in the polyneuropathy associated with familial amyloid polyneuropathy after liver transplantation.
Neurology 1998;51(3):926-7.
1998: Ole B Suhr; Yukio Ando; Per-Ingvar Ohlsson; Anders Olofsson; Karin Andersson; Erik Lundgren; Masayuki Ando; Gösta Holmgren
Investigation into thiol conjugation of transthyretin in hereditary transthyretin amyloidosis.
European journal of clinical investigation 1998;28(8):687-92.
1998: Yukio Ando; Intissar Anan; Ole B Suhr; Gösta Holmgren; Paulo Costa
Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy.
BMJ (Clinical research ed.) 1998;316(7143):1500-1.
1998: P Pekkarinen; Iiris Hovatta; Panu Hakola; O Järvi; Marjo Kestilä; U Lenkkeri; Rolf Adolfsson; Gösta Holmgren; Per-Olof Nylander; Lisbeth Tranebjaerg; Joseph D Terwilliger; Jouko Lönnqvist; Leena Peltonen
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.
American journal of human genetics 1998;62(2):362-72.
1998: Jens Johansson; Lars Forsgren; Ola Sandgren; Alexis Brice; Gösta Holmgren; M Holmberg
Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.
Human molecular genetics 1998;7(2):171-6.
1998: Erik Forestier; Gösta Holmgren; Göran Roos
Flow cytometric DNA index and karyotype in childhood lymphoblastic leukemia.
Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology 1998;17(3):145-56.
1998: Ole B Suhr; Yukio Ando; Gösta Holmgren; Lars Wikström; Styrbjörn Friman; Gustaf Herlenius; Bo-Göran Ericzon
Liver transplantation in familial amyloidotic polyneuropathy (FAP). A comparative study of transplanted and non-transplanted patient's survival.
Transplant international : official journal of the European Society for Organ Transplantation 1998;11 Suppl 1():S160-3.
1997: Yukio Ando; Ole B Suhr; Takeshi Yamashita; Per-Ingvar Ohlsson; Gösta Holmgren; Konen Obayashi; Hisayasu Terazaki; C Mambule; Makoto Uchino; Masayuki Ando
Detection of different forms of variant transthyretin (Met30) in cerebrospinal fluid.
Neuroscience letters 1997;238(3):123-6.
1997: A Sillén; Gösta Holmgren; Claes Wadelius
First prenatal diagnosis by mutation analysis in a family with Sjögren-Larsson syndrome.
Prenatal diagnosis 1997;17(12):1147-9.
1997: C Graff; A Eriksson; Kristina Forsman; Ola Sandgren; Gösta Holmgren; Claes Wadelius
Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids.
Human genetics 1997;101(3):263-70.
1997: I Ranløv; Yukio Ando; Per-Ingvar Ohlsson; Gösta Holmgren; PJ Ranløv; Ole B Suhr
Rapid screening for amyloid-related variant forms of transthyretin is possible by electrospray ionization mass spectrometry.
European journal of clinical investigation 1997;27(11):956-9.
1997: Herbert Sandstrom; Ake Wahlin; M Eriksson; Gösta Holmgren; L Lind; Ola Sandgren
Angioid streaks are part of a familial syndrome of dyserythropoietic anaemia (CDA III).
British journal of haematology 1997;98(4):845-9.
1997: Mary MacDougall; BR DuPont; Darrin Simmons; BE Reus; PH Krebsbach; C Kärrman; Gösta Holmgren; Robin J Leach; Kristina Forsman
Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21.
Genomics 1997;41(1):115-8.
1997: Yukio Ando; N Nyhlin; Ole B Suhr; Gösta Holmgren; K Uchida; M el Sahly; Takeshi Yamashita; H Terasaki; Masaaki Nakamura; Makoto Uchino; Masayuki Ando
Oxidative stress is found in amyloid deposits in systemic amyloidosis.
Biochemical and biophysical research communications 1997;232(2):497-502.
1997: C Kärrman; Birgitta Bäckman; M Dixon; Gösta Holmgren; Kristina Forsman
Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21.
Genomics 1997;39(2):164-70.
1996: L Forsgren; R Libelius; M Holmberg; Ulrika von Döbeln; R Wibom; J Heijbel; Ola Sandgren; Gösta Holmgren
Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1.
Journal of the neurological sciences 1996;144(1-2):91-8.
1996: Yukio Ando; Per-Ingvar Ohlsson; Ole B Suhr; N Nyhlin; Takeshi Yamashita; Gösta Holmgren; A Danielsson; Ola Sandgren; Makoto Uchino; Masayuki Ando
A new simple and rapid screening method for variant transthyretin-related amyloidosis.
Biochemical and biophysical research communications 1996;228(2):480-3.
1996: H K Blomquist; N Dahl; L Gustafsson; C Hellerud; E Holme; Gösta Holmgren; L Matsson; M von Zweigbergk
Glycerol kinase deficiency in two brothers with and without clinical manifestations.
Clinical genetics 1996;50(5):375-9.
1996: C Kärrman; B Bäckman; Gösta Holmgren; Kristina Forsman
Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q.
Archives of oral biology 1996;41(8-9):893-900.
1995: J Balciuniene; K Johansson; Ola Sandgren; L Wachtmeister; Gösta Holmgren; Kristina Forsman
A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13.
Genomics 1995;30(2):281-6.
1995: Ole B Suhr; Gösta Holmgren; L Steen; L Wikström; G Norden; S Friman; Frans Duraj; Carl G Groth; Bo-Göran Ericzon
Liver transplantation in familial amyloidotic polyneuropathy. Follow-up of the first 20 Swedish patients.
Transplantation 1995;60(9):933-8.
1995: Gösta Holmgren; L Ozelius; L Forsgren; B G Almay; M Holmberg; Patricia L Kramer; Stanley Fahn; X O Breakefield
Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.
Journal of neurology, neurosurgery, and psychiatry 1995;59(2):178-81.
1995: M Holmberg; J Johansson; L Forsgren; J Heijbel; Ola Sandgren; Gösta Holmgren
Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.
Human molecular genetics 1995;4(8):1441-5.
1995: U Drugge; M Holmberg; Gösta Holmgren; B G Almay; H Linderholm
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.
Journal of medical genetics 1995;32(5):344-7.
1995: Bo-Göran Ericzon; Ole B Suhr; Ulrika Broomé; Gösta Holmgren; Frans Duraj; L Eleborg; L Wikström; G Norden; S Friman; Carl G Groth
Liver transplantation halts the progress of familial amyloidotic polyneuropathy.
Transplantation proceedings 1995;27(1):1233.
1995: L Lind; Herbert Sandstrom; Ake Wahlin; M Eriksson; B Nilsson-Sojka; Carin Sikström; Gösta Holmgren
Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25.
Human molecular genetics 1995;4(1):109-12.
1994: C Graff; Kristina Forsman; C Larsson; S Nordström; L Lind; K Johansson; Ola Sandgren; J Weissenbach; Gösta Holmgren; Karl-Henrik Gustavson
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci.
Genomics 1994;24(3):425-34.
1994: L Lind; A Lundström; P A Hofer; Gösta Holmgren
The gene for diffuse palmoplantar keratoderma of the type found in northern Sweden is localized to chromosome 12q11-q13.
Human molecular genetics 1994;3(10):1789-93.
1994: Kristina Forsman; L Lind; B Bäckman; E Westermark; Gösta Holmgren
Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.
Human molecular genetics 1994;3(9):1621-5.
1994: B H Holmberg; Gösta Holmgren; E Nelis; Christine Van Broeckhoven; B Westerberg
Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2.
Journal of medical genetics 1994;31(6):435-41.
1994: Ole B Suhr; A Danielsson; Gösta Holmgren; L Steen
Malnutrition and gastrointestinal dysfunction as prognostic factors for survival in familial amyloidotic polyneuropathy.
Journal of internal medicine 1994;235(5):479-85.
1994: Gösta Holmgren; P M Costa; C Andersson; K Asplund; L Steen; L Beckman; Per-Olof Nylander; A Teixeira; Maria João Saraiva; Paulo Costa
Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate.
Journal of medical genetics 1994;31(5):351-4.
1994: Michael Binzer; L Forsgren; Gösta Holmgren; U Drugge; Sten Fredrikson
Familial clustering of multiple sclerosis in a northern Swedish rural district.
Journal of neurology, neurosurgery, and psychiatry 1994;57(4):497-9.
1994: Jan Wahlström; Laurie J Ozelius; Patricia L Kramer; Mårten Kyllerman; D Schuback; L Forsgren; Gösta Holmgren; U Drugge; G Sanner; Stanley Fahn
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.
Clinical genetics 1994;45(2):88-92.
1993: A Sousa; R Andersson; U Drugge; Gösta Holmgren; Ola Sandgren
Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence.
Human heredity 1993;43(5):288-94.
1993: Mårten Kyllerman; G Sanner; L Forsgren; Gösta Holmgren; Jan Wahlström
Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia.
Brain & development 1993;15(4):295-8.
1993: U Drugge; R Andersson; F Chizari; M Danielsson; Gösta Holmgren; Ola Sandgren; A Sousa
Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis.
Journal of medical genetics 1993;30(5):388-92.
1993: Gösta Holmgren; B G Ericzon; C G Groth; L Steen; Ole B Suhr; O Andersen; B G Wallin; A Seymour; S Richardson; P N Hawkins
Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis.
Lancet 1993;341(8853):1113-6.
1993: J A Hamilton; LK Steinrauf; Bradford C Braden; Juris J Liepnieks; Merrill D Benson; Gösta Holmgren; Ola Sandgren; L Steen
The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution.
The Journal of biological chemistry 1993;268(4):2416-24.
1993: Klaus L Leenders; P Hartvig; L Forsgren; Gösta Holmgren; B Almay; S A Eckernäs; H Lundqvist; B Långström
Striatal [11C]-N-methyl-spiperone binding in patients with focal dystonia (torticollis) using positron emission tomography.
Journal of neural transmission. Parkinson's disease and dementia section 1993;5(2):79-87.
1992: Kristina Forsman; C Graff; S Nordström; K Johansson; E Westermark; E Lundgren; Karl-Henrik Gustavson; Claes Wadelius; Gösta Holmgren
The gene for Best's macular dystrophy is located at 11q13 in a Swedish family.
Clinical genetics 1992;42(3):156-9.
1992: J A Hamilton; LK Steinrauf; Juris J Liepnieks; Merrill D Benson; Gösta Holmgren; Ola Sandgren; L Steen
Alteration in molecular structure which results in disease: the Met-30 variant of human plasma transthyretin.
Biochimica et biophysica acta 1992;1139(1-2):9-16.
1992: U Drugge; Gösta Holmgren; H K Blomquist; N Dahl; Karl-Henrik Gustavson; H Malmgren
Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuries.
American journal of medical genetics 1992;43(1-2):353-4.
1992: U Drugge; Gösta Holmgren; B Udd
The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish population.
Human heredity 1992;42(3):184-8.
1992: Gösta Holmgren; S Bergström; U Drugge; E Lundgren; C Nording-Sikström; Ola Sandgren; L Steen
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Clinical genetics 1992;41(1):39-41.
1991: Ola Sandgren; U Drugge; Gösta Holmgren; A Sousa
Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
Clinical genetics 1991;40(6):452-60.
1991: Gösta Holmgren; L Steen; J Ekstedt; C G Groth; B G Ericzon; S Eriksson; O Andersen; I Karlberg; G Nordén; M Nakazato
Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30).
Clinical genetics 1991;40(3):242-6.
1991: D Schuback; Patricia L Kramer; Laurie J Ozelius; Gösta Holmgren; L Forsgren; Mårten Kyllerman; Jan Wahlström; C M Craft; TG Nygaard; M Brin
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.
Human genetics 1991;87(3):311-6.
1991: U Drugge; H K Blomquist; Karl-Henrik Gustavson; Gösta Holmgren
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth century.
American journal of medical genetics 1991;38(2-3):363-6.
1990: Ola Sandgren; Gösta Holmgren; E Lundgren
Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
Archives of ophthalmology 1990;108(11):1584-6.
1990: Anders Fasth; Erik Forestier; E Holmberg; Gösta Holmgren; I Nordenson; T Söderström; Jan Wahlström
Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity?
Acta paediatrica Scandinavica 1990;79(6-7):605-12.
1990: Mårten Kyllerman; L Forsgren; G Sanner; Gösta Holmgren; Jan Wahlström; U Drugge
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation.
Movement disorders : official journal of the Movement Disorder Society 1990;5(4):270-9.
1989: I Nordenson; L Bjermer; Gösta Holmgren; P Hörnsten; Ake Wahlin
t(6;9) in bone marrow cells in two patients with sarcoidosis and acute myeloid leukemia.
Cancer genetics and cytogenetics 1989;38(2):297-300.
1988: Gösta Holmgren; U Drugge; E Lundgren; Ola Sandgren; L Steen
[Identification of genetic carriers in familial amyloidosis with polyneuropathy is possible with the DNA technic].
Läkartidningen 1988;85(44):3677-9.
1988: Gösta Holmgren; E Haettner; I Nordenson; Ola Sandgren; L Steen; E Lundgren
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Clinical genetics 1988;34(5):333-8.
1988: Ola Sandgren; Gösta Holmgren; E Lundgren; L Steen
Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis.
Archives of ophthalmology 1988;106(6):790-2.
1988: Gösta Holmgren; H K Blomquist; U Drugge; Karl-Henrik Gustavson
Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th century.
American journal of medical genetics 1988;30(1-2):673-9.
1988: Gösta Holmgren; E Holmberg; Anton Lindström; E Lindström; I Nordenson; Ola Sandgren; L Steen; B Svensson; E Lundgren; A von Gabain
Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis.
Clinical genetics 1988;33(3):176-80.
1988: L Forsgren; Gösta Holmgren; B G Almay; U Drugge
Autosomal dominant torsion dystonia in a Swedish family.
Advances in neurology 1988;50():83-92.
1988: I Nordenson; B A Adrian; Gösta Holmgren; Göran Roos; O Rudolphi; Y Wahlqvist; Erik Forestier
Near-haploidy in childhood leukemia: a high-risk component.
Pediatric hematology and oncology 1988;5(4):309-14.
1987: Gösta Holmgren
Aspects of prenatal prevention.
Upsala journal of medical sciences. Supplement 1987;44():226-30.
1987: Karl-Henrik Gustavson; Gösta Holmgren; H K Blomquist
Chromosomal aberrations in mildly mentally retarded children in a northern Swedish county.
Upsala journal of medical sciences. Supplement 1987;44():165-8.
1985: H K Blomquist; M Bohman; S O Edvinsson; C Gillberg; K H Gustavson; Gösta Holmgren; J Wahlström
Frequency of the fragile X syndrome in infantile autism. A Swedish multicenter study.
Clinical genetics 1985;27(2):113-7.