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Hans Goebel

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Hans H Goebel; Harald D Müller
Storage diseases: diagnostic position.
Hans H Goebel; Werner Stenzel
Practical application of electron microscopy to neuromuscular diseases.
Hans H Goebel
When tubules aggregate.

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2013: Hans H Goebel; Harald D Müller
Storage diseases: diagnostic position.
Ultrastructural pathology 2013;37(1):19-22.
2013: Hans H Goebel; Werner Stenzel
Practical application of electron microscopy to neuromuscular diseases.
Ultrastructural pathology 2013;37(1):15-8.
2012: Hans H Goebel
When tubules aggregate.
Neuromuscular disorders : NMD 2012;22(3):208-10.
2011: Hans H Goebel
Neuropathology of neurometabolic diseases in children with epilepsy.
Brain & development 2011;33(9):726-33.
2011: Hans H Goebel; Carsten G Bönnemann
169th ENMC International Workshop Rare Structural Congenital Myopathies 6-8 November 2009, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2011;21(5):363-74.
2009: Hans H Goebel; Harald D Müller; R Schröder
[Congenital and other myopathies].
Der Pathologe 2009;30(5):365-9.
2009: Harald D Müller; F K H van Landeghem; P F Schmidt; Clemens Sommer; Hans H Goebel
Macrophagic myofasciitis plus (distinct types of muscular dystrophy).
Neuropediatrics 2009;40(4):174-8.
2009: Hans H Goebel; Nigel G Laing
Actinopathies and myosinopathies.
Brain pathology (Zurich, Switzerland) 2009;19(3):516-22.
2009: Hans H Goebel
Protein aggregate myopathies. Introduction.
Brain pathology (Zurich, Switzerland) 2009;19(3):480-2.
2009: Alexey Shatunov; Montse Olivé; Zagaa Odgerel; Christine Stadelmann-Nessler; Kerstin Irlbacher; Frank van Landeghem; Munkhuu Bayarsaikhan; Hee-Suk Lee; Bertrand Goudeau; Patrick F Chinnery; Volker Straub; David Hilton-Jones; Maxwell S Damian; Anna Kaminska; Patrick Vicart; Kate Bushby; Marinos C Dalakas; Nyamkhishig Sambuughin; Isidro Ferrer; Hans H Goebel; Lev G Goldfarb
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.
European journal of human genetics : EJHG 2009;17(5):656-63.
2009: Christoph S Clemen; Dirk Fischer; Jens Reimann; Ludwig Eichinger; Clemens R Müller; Harald D Müller; Hans H Goebel; Rolf Schröder
How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathy.
Human mutation 2009;30(3):E490-9.
2008: Hans H Goebel; Michel Fardeau; Montse Olivé; Rolf Schröder
156th ENMC International Workshop: desmin and protein aggregate myopathies, 9-11 November 2007, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2008;18(7):583-92.
2007: Hans H Goebel
Cap disease uncapped.
Neuromuscular disorders : NMD 2007;17(6):429-32.
2006: Hans H Goebel; Harald D Müller
Protein aggregate myopathies.
Seminars in pediatric neurology 2006;13(2):96-103.
2006: Hans H Goebel; Knut Brockman; Carsten G Bönnemann; Irene A P Warlo; Folker Hanefeld; Siegfried Labeit; Hayley J Durling; Nigel G Laing
Patient with actin aggregate myopathy and not formerly identified ACTA1 mutation is heterozygous for the Gly15Arg mutation of ACTA1, which has previously been associated with actinopathy.
Journal of child neurology 2006;21(6):545.
2006: Danielle E Dye; Biagio Azzarelli; Hans H Goebel; Nigel G Laing
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred.
Neuromuscular disorders : NMD 2006;16(6):357-60.
2005: Tatiana Foroud; Nathan Pankratz; A P Batchman; Michael W Pauciulo; Ruben Vidal; Leticia Miravalle; Hans H Goebel; Lisa J Cushman; Biagio Azzarelli; H Horak; Martin R Farlow; William C Nichols
A mutation in myotilin causes spheroid body myopathy.
Neurology 2005;65(12):1936-40.
2005: Mehar Chand Sharma; Christoph Schultze; Arpad von Moers; Gisela Stoltenburg-Didinger; Yoon S Shin; Teodor Podskarbi; Klaus Isenhardt; Dominique S Tews; Hans H Goebel
Delayed or late-onset type II glycogenosis with globular inclusions.
Acta neuropathologica 2005;110(2):151-7.
2005: Alexandra Vrabie; Lev G Goldfarb; Alexey Shatunov; Andrea Nägele; Peter Fritz; Ingo Kaczmarek; Hans H Goebel
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation.
Acta neuropathologica 2005;109(4):411-7.
2005: Nigel G Laing; Chantal Ceuterick-de Groote; Danielle E Dye; Khema Liyanage; Rachael M Duff; Bruno Dubois; W Robberecht; R Sciot; Jean-Jacques Martin; Hans H Goebel
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases.
Neurology 2005;64(3):527-9.
2005: Hans H Goebel
Congenital myopathies in the new millennium.
Journal of child neurology 2005;20(2):94-101.
2004: Hans H Goebel
The Eighth Meryon Society Lecture read at Worcester College, Oxford on 2 July, 2004.
Neuromuscular disorders : NMD 2004;14(12):822-8.
2004: Hans H Goebel; Michel Fardeau
121st ENMC International Workshop on Desmin and Protein Aggregate Myopathies. 7-9 November 2003, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2004;14(11):767-73.
2004: Carina Wallgren-Pettersson; Katarina Pelin; Kristen J Nowak; Francesco Muntoni; Norma B Romero; Hans H Goebel; Kathryn N North; Alan H Beggs; Nigel G Laing
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin.
Neuromuscular disorders : NMD 2004;14(8-9):461-70.
2004: Ana Ferreiro; Chantal Ceuterick-de Groote; Jared J Marks; Nathalie Goemans; Gudrun Schreiber; Folker Hanefeld; Michel Fardeau; Jean-Jacques Martin; Hans H Goebel; Pascale Richard; Pascale Guicheney; Carsten G Bönnemann
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.
Annals of neurology 2004;55(5):676-86.
2004: Hans H Goebel; Knut Brockmann; Carsten G Bönnemann; Irene A P Warlo; Folker Hanefeld; Siegfried Labeit; Hayley J Durling; Nigel G Laing
Actin-related myopathy without any missense mutation in the ACTA1 gene.
Journal of child neurology 2004;19(2):149-53.
2004: Ayush Dagvadorj; Montse Olivé; Jean-Andoni Urtizberea; Martin Halle; Alexey Shatunov; Carsten G Bönnemann; Kye-Yoon Park; Hans H Goebel; Isidro Ferrer; Patrick Vicart; Marinos C Dalakas; Lev G Goldfarb
A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.
Journal of neurology 2004;251(2):143-9.
2004: Hans H Goebel; Krystyna E Wisniewski
Current state of clinical and morphological features in human NCL.
Brain pathology (Zurich, Switzerland) 2004;14(1):61-9.
2003: Hans H Goebel
Congenital myopathies at their molecular dawning.
Muscle & nerve 2003;27(5):527-48.
2002: Hans H Goebel; Michel Fardeau
Desmin - Protein Surplus Myopathies, 96th European Neuromuscular Centre (ENMC)-sponsored International Workshop held 14-16 September 2001, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2002;12(7-8):687-92.
2002: Hans H Goebel; Astrid Borchert
Protein surplus myopathies and other rare congenital myopathies.
Seminars in pediatric neurology 2002;9(2):160-70.
2002: Kristian Donner; Miina Ollikainen; Maaret Ridanpää; Hans-Jürgen Christen; Hans H Goebel; Marianne de Visser; Katarina Pelin; Carina Wallgren-Pettersson
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.
Neuromuscular disorders : NMD 2002;12(2):151-8.
2001: Hans H Goebel; L E Halbig; Lev G Goldfarb; Ralf Schober; M Albani; E Neuen-Jacob; T Voit
Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathy.
Neuropediatrics 2001;32(4):196-205.
2001: Hans H Goebel
The 8th International Congress on Neuronal Ceroid Lipofuscinoses (Batten disease)--NCL 2000, 20-24 September, 2000, Oxford, United Kingdom.
Brain pathology (Zurich, Switzerland) 2001;11(2):259-60.
2001: Hans H Goebel; E Kominami; E Neuen-Jacob; R B Wheeler
Morphological studies on CLN2.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2001;5 Suppl A():203-7.
2001: Hans H Goebel; Alfried Kohlschuetter
Dementia in the neuronal ceroid-lipofuscinoses.
Advances in experimental medicine and biology 2001;487():211-7.
2001: Hans H Goebel; Irene A P Warlo
Surplus protein myopathies.
Neuromuscular disorders : NMD 2001;11(1):3-6.
2000: Kye-Yoon Park; Marinos C Dalakas; Hans H Goebel; V J Ferrans; Cristina Semino-Mora; S Litvak; Kazuyo Takeda; Lev G Goldfarb
Desmin splice variants causing cardiac and skeletal myopathy.
Journal of medical genetics 2000;37(11):851-7.
2000: Hans H Goebel
The new nosography of the neuronal ceroid-lipofuscinoses.
Annales de pathologie 2000;20(5):479-91.
2000: Hans H Goebel; Irene A P Warlo
Progress in desmin-related myopathies.
Journal of child neurology 2000;15(9):565-72.
2000: Hans H Goebel; Irene A P Warlo
Gene-related protein surplus myopathies.
Molecular genetics and metabolism 2000;71(1-2):267-75.
2000: Hans H Goebel
Morphological aspects of the neuronal ceroid lipofuscinoses.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2000;21(3 Suppl):S27-33.
1999: Susann Seddigh; Norbert Dahmen; Hans H Goebel; Hanns C Hopf; Merrill D Benson
[Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy].
Der Nervenarzt 1999;70(10):899-902.
1999: Hans H Goebel
Extracerebral biopsies in neurodegenerative diseases of childhood.
Brain & development 1999;21(7):435-43.
1999: Kristen J Nowak; Duangrurdee Wattanasirichaigoon; Hans H Goebel; M Wilce; Katarina Pelin; Kristian Donner; Rebecca L Jacob; Christoph Hübner; K Oexle; J R Anderson; C M Verity; Kathryn N North; Susan T Iannaccone; C R Müller; P Nürnberg; Francesco Muntoni; Caroline Sewry; I Hughes; Rebecca Sutphen; A G Lacson; Kathryn J Swoboda; J Vigneron; Carina Wallgren-Pettersson; Alan H Beggs; Nigel G Laing
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
Nature genetics 1999;23(2):208-12.
1999: Benedikt Schoser; A Faissner; Hans H Goebel
Immunolocalization of tenascin-C in human type II fiber atrophy.
Journal of molecular neuroscience : MN 1999;13(1-2):167-75.
1999: Rolf Schröder; Irene A P Warlo; Harald Herrmann; Peter F.M. van der Ven; C Klasen; Ingmar Blümcke; Rustam R Mundegar; Dieter O Fürst; Hans H Goebel; Thomas M Magin
Immunogold EM reveals a close association of plectin and the desmin cytoskeleton in human skeletal muscle.
European journal of cell biology 1999;78(4):288-95.
1999: Hans H Goebel; Sydney S Schochet; ME Jaynes; W Brück; Alfried Kohlschuetter; Faycal Hentati
Progress in neuropathology of the neuronal ceroid lipofuscinoses.
Molecular genetics and metabolism 1999;66(4):367-72.
1999: Hans H Goebel; J R Anderson
Structural congenital myopathies (excluding nemaline myopathy, myotubular myopathy and desminopathies): 56th European Neuromuscular Centre (ENMC) sponsored International Workshop. December 12-14, 1997, Naarden, The Netherlands.
Neuromuscular disorders : NMD 1999;9(1):50-7.
1998: Dominique S Tews; Hans H Goebel
Cell death and oxidative damage in inflammatory myopathies.
Clinical immunology and immunopathology 1998;87(3):240-7.
1998: Hans H Goebel
Congenital myopathies with inclusion bodies: a brief review.
Neuromuscular disorders : NMD 1998;8(3-4):162-8.
1998: Hans H Goebel; Sydney S Schochet; ME Jaynes; L Gutmann
Ultrastructure of the retina in adult neuronal ceroid lipofuscinosis.
Acta anatomica 1998;162(2-3):127-32.
1998: Hans H Goebel; J D Sharp
The neuronal ceroid-lipofuscinoses. Recent advances.
Brain pathology (Zurich, Switzerland) 1998;8(1):151-62.
1998: Hans H Goebel; B D Lake
Lysosomal and peroxisomal disorders. Recent advances: introduction.
Brain pathology (Zurich, Switzerland) 1998;8(1):73-8.
1997: Dominique S Tews; Hans H Goebel; H M Meinck
DNA-fragmentation and apoptosis-related proteins of muscle cells in motor neuron disorders.
Acta neurologica Scandinavica 1997;96(6):380-6.
1997: Dominique S Tews; Hans H Goebel; I Schneider; A Gunkel; Eberhard Stennert; Wolfram F Neiss
Expression of different isoforms of nitric oxide synthase in experimentally denervated and reinnervated skeletal muscle.
Journal of neuropathology and experimental neurology 1997;56(12):1283-9.
1997: Hans H Goebel
Desmin-related myopathies.
Current opinion in neurology 1997;10(5):426-9.
1997: Hans H Goebel; A N D'Agostino; J Wilson; G Cole; T Foroud; D Koller; Martin R Farlow; Biagio Azzarelli; J Muller
Spheroid body myopathy revisited.
Muscle & nerve 1997;20(9):1127-36.
1997: Dominique S Tews; Hans H Goebel
DNA-fragmentation and expression of apoptosis-related proteins in muscular dystrophies.
Neuropathology and applied neurobiology 1997;23(4):331-8.
1997: Dominique S Tews; Hans H Goebel; I Schneider; A Gunkel; Eberhard Stennert; Wolfram F Neiss
Expression profile of stress proteins, intermediate filaments, and adhesion molecules in experimentally denervated and reinnervated rat facial muscle.
Experimental neurology 1997;146(1):125-34.
1997: Dominique S Tews; Hans H Goebel; R R Heffner; Bernd Reitter; T Vetter; K F Kreitner
Hamartoma of the triceps surae muscle.
Acta neuropathologica 1997;94(1):91-4.
1997: Hans H Goebel; Susann Seddigh; Hanns C Hopf; T Uemichi; Merrill D Benson; Victor A McKusick
A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathy.
Neuromuscular disorders : NMD 1997;7(4):229-30.
1997: Hans H Goebel; J R Anderson; Christoph Hübner; K Oexle; Irene A P Warlo
Congenital myopathy with excess of thin myofilaments.
Neuromuscular disorders : NMD 1997;7(3):160-8.
1997: Hans H Goebel; R Meyermann; R Rosin; W Schlote
Characteristic morphologic manifestation of CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, in skeletal muscle and skin.
Muscle & nerve 1997;20(5):625-7.
1997: Dominique S Tews; Hans H Goebel; I Schneider; A Gunkel; Eberhard Stennert; Wolfram F Neiss
DNA-fragmentation and expression of apoptosis-related proteins in experimentally denervated and reinnervated rat facial muscle.
Neuropathology and applied neurobiology 1997;23(2):141-9.
1997: Hans H Goebel
Morphologic diagnosis in neuronal ceroid lipofuscinosis.
Neuropediatrics 1997;28(1):67-9.
1997: Dominique S Tews; Hans H Goebel
Apoptosis-related proteins in skeletal muscle fibers of spinal muscular atrophy.
Journal of neuropathology and experimental neurology 1997;56(2):150-6.
1997: Hans H Goebel; Irene A P Warlo
Nemaline myopathy with intranuclear rods--intranuclear rod myopathy.
Neuromuscular disorders : NMD 1997;7(1):13-9.
1997: Hans H Goebel; A Piirsoo; Irene A P Warlo; O Schofer; S Kehr; M Gaude
Infantile intranuclear rod myopathy.
Journal of child neurology 1997;12(1):22-30.
1996: Hans H Goebel
The neuronal ceroid-lipofuscinoses.
Seminars in pediatric neurology 1996;3(4):270-8.
1996: Hans H Goebel; M Fardeau
Familial desmin-related myopathies and cardiomyopathies--from myopathology to molecular and clinical genetics. 36th European Neuromuscular Center (ENMC)-Sponsored International Workshop 20-22 October, 1995, Naarden, The Netherlands.
Neuromuscular disorders : NMD 1996;6(5):383-8.
1996: Dominique S Tews; Hans H Goebel
Inflammatory myopathies.
Current opinion in neurology 1996;9(5):375-9.
1996: Dominique S Tews; Hans H Goebel
DNA fragmentation and BCL-2 expression in infantile spinal muscular atrophy.
Neuromuscular disorders : NMD 1996;6(4):265-73.
1996: Hans H Goebel; L Gerhard; E Kominami; M Haltia
Neuronal ceroid-lipofuscinosis--late-infantile or Jansky-Bielschowsky type--revisited.
Brain pathology (Zurich, Switzerland) 1996;6(3):225-8.
1996: Hans H Goebel
Congenital myopathies.
Seminars in pediatric neurology 1996;3(2):152-61.
1996: Bernd Reitter; Hans H Goebel
Dystrophinopathies.
Seminars in pediatric neurology 1996;3(2):99-109.
1996: Dominique S Tews; Hans H Goebel
Cytokine expression profile in idiopathic inflammatory myopathies.
Journal of neuropathology and experimental neurology 1996;55(3):342-7.
1996: A Bornemann; R Besser; Y S Shin; Hans H Goebel
A mild adult myopathic variant of type IV glycogenosis.
Neuromuscular disorders : NMD 1996;6(2):95-9.
1995: Hans H Goebel
The neuronal ceroid-lipofuscinoses.
Journal of child neurology 1995;10(6):424-37.
1995: Hans H Goebel
Desmin-related neuromuscular disorders.
Muscle & nerve 1995;18(11):1306-20.
1995: B C Kieseier; Hans H Goebel
Immunelectronmicroscopic characterization of T4 and T8 lymphocytes and natural killer cells in neuronal ceroid-lipofuscinosis.
American journal of medical genetics 1995;57(2):222-4.
1995: Hans H Goebel; Irene A P Warlo; T Klockgether; Klaus Harzer
Significance of lipopigments with fingerprint profiles in eccrine sweat gland epithelial cells.
American journal of medical genetics 1995;57(2):187-90.
1995: Hans H Goebel; F Gullotta; T Bajanowski; F J Hansen; Heiko Braak
Pigment variant of neuronal ceroid-lipofuscinosis.
American journal of medical genetics 1995;57(2):155-9.
1995: Dominique S Tews; Hans H Goebel
Expression of cell adhesion molecules in inflammatory myopathies.
Journal of neuroimmunology 1995;59(1-2):185-94.
1995: Ernst Hund; R Heckl; Hans H Goebel; Hans-Michael Meinck
Inclusion body myositis presenting with isolated erector spinae paresis.
Neurology 1995;45(5):993-4.
1995: Wolfgang M Franz; M Cremer; R Herrmann; E Grünig; W Fogel; T Scheffold; Hans H Goebel; R Kircheisen; Wolfgang Kübler; T Voit
X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene.
Annals of the New York Academy of Sciences 1995;752():470-91.
1995: Hans H Goebel; M Fardeau
Desmin in myology. 24th European Neuromuscular Center-sponsored workshop held 5-6 November 1993, Naarden, The Netherlands.
Neuromuscular disorders : NMD 1995;5(2):161-6.
1995: Hans H Goebel; J Vesa; Bernd Reitter; T O Goecke; B Schneider-Rätzke; E Merz
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach.
Brain & development 1995;17(2):83-8.
1994: Eberhard Stennert; C Böschen; A Gunkel; Hans H Goebel
Effects of electrostimulation therapie: enzyme-histological and myometric changes in the denervated musculature.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 1994;():S37-41.
1994: Hans H Goebel; I Schneider; Dominique S Tews; A Gunkel; Eberhard Stennert; Wolfram F Neiss
Morphologic studies on human and rodent facial muscles.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 1994;():S24-7.
1994: B C Kieseier; Hans H Goebel
Characterization of T-cell subclasses and NK-cells in lysosomal disorders by immuno-electron microscopy.
Neuropathology and applied neurobiology 1994;20(6):604-8.
1994: LM Drach; Jürgen R E Bohl; Hans H Goebel
The lipofuscin content of nerve cells of the inferior olivary nucleus in Alzheimer's disease.
Dementia (Basel, Switzerland) 1994;5(5):234-9.
1994: Hans H Goebel
Prenatal ultrastructural diagnosis in the neuronal ceroid-lipofuscinoses.
Pathology, research and practice 1994;190(7):728-33.
1994: Hans H Goebel; G Husmann; T Voit; M Calişkan
Special techniques in diagnostic myopathology.
The Turkish journal of pediatrics 1994;36(3):223-37.
1994: Hans H Goebel; T Voit; Irene A P Warlo; K Jacobs; U Johannsen; C R Müller
Immunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathy.
Revue neurologique 1994;150(6-7):452-9.
1994: Hans H Goebel
The Second International Duodecim Symposium on Molecular Biology of Lysosomal Diseases, in Majvik, Finland, May 23-26, 1993.
Brain pathology (Zurich, Switzerland) 1994;4(2):199-200.
1994: Dominique S Tews; Hans H Goebel; I Schneider; A Gunkel; Eberhard Stennert; Wolfram F Neiss
Morphology of experimentally denervated and reinnervated rat facial muscle. I. Histochemical and histological findings.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 1994;251(1):36-40.
1993: A Bornemann; Jürgen R E Bohl; Otto Hey; S Störkel; H Gamm; Wibke Müller-Forell; Axel Perneczky; Hans H Goebel
Amyloidoma of the gasserian ganglion as a cause of symptomatic neuralgia of the trigeminal nerve: report of three cases.
Journal of neurology 1993;241(1):10-4.
1993: Hans H Goebel; S Kimura; Klaus Harzer; H Klein
Ultrastructural pathology of eccrine sweat gland epithelial cells in globoid cell leukodystrophy.
Journal of child neurology 1993;8(2):171-4.
1993: NJ Hopf; Hans H Goebel
Experimental emetine myopathy: enzyme histochemical, electron microscopic, and immunomorphological studies.
Acta neuropathologica 1993;85(4):414-8.
1993: Hans H Goebel; J Lehmann
An ultrastructural study of the retina in human late infantile neuroaxonal dystrophy.
Retina (Philadelphia, Pa.) 1993;13(1):50-5.
1993: Hans H Goebel
Protracted juvenile neuronal ceroid-lipofuscinosis.
Journal of inherited metabolic disease 1993;16(2):233-6.
1993: Hans H Goebel; A Bornemann
Desmin pathology in neuromuscular diseases.
Virchows Archiv. B, Cell pathology including molecular pathology 1993;64(3):127-35.
1992: Hans H Goebel
Neuronal ceroid-lipofuscinoses: the current status.
Brain & development 1992;14(4):203-11.
1992: Hans H Goebel
Retina in various animal models of neuronal ceroid-lipofuscinosis.
American journal of medical genetics 1992;42(4):605-8.
1992: Hans H Goebel; H Busch-Hettwer; J Bohl
Ultrastructural study of the retina in late infantile metachromatic leukodystrophy.
Ophthalmic research 1992;24(2):103-9.
1992: Hans H Goebel; Y S Shin; F Gullotta; T Yokota; J Alroy; T Voit; P Haller; A Schulz
Adult polyglucosan body myopathy.
Journal of neuropathology and experimental neurology 1992;51(1):24-35.
1991: U Horn; Hans H Goebel; S Störkel; J Bohl; E Thomas; W Schlote; G Budzilovich
Immunohistochemistry of amyloid-related neuropathies.
Clinical neuropathology 1991;10(5):237-43.
1991: R Wolf; Hans H Goebel; L Gutmann; S Schochet
Capillaries within human skeletal muscle fibers.
Pathology, research and practice 1991;187(7):857-63.
1991: W Brück; Hans H Goebel; P Dienes
B and T lymphocytes are affected in lysosomal disorders--an immunoelectron microscopic study.
Neuropathology and applied neurobiology 1991;17(3):219-22.
1991: Hans H Goebel
Congenital myopathies.
Acta paediatrica Japonica; Overseas edition 1991;33(2):247-55.
1991: L Halbig; Hans H Goebel; H C Hopf; Roland Moll
Spheroid-cytoplasmic complexes in a congenital myopathy.
Revue neurologique 1991;147(4):300-7.
1990: Hans H Goebel; Klaus Harzer; J P Ernst; J Bohl; H Klein
Late-onset globoid cell leukodystrophy: unusual ultrastructural pathology and subtotal beta-galactocerebrosidase deficiency.
Journal of child neurology 1990;5(4):299-307.
1990: Hans H Goebel; I Döpfmer
An ultrastructural study on retinal neural and pigment epithelial cells in ovine neuronal ceroid-lipofuscinosis.
Ophthalmic paediatrics and genetics 1990;11(1):61-9.
1990: Hans H Goebel; P F Schmidt; J Bohl; B Tettenborn; G Krämer; L Gutmann
Polyneuropathy due to acute arsenic intoxication: biopsy studies.
Journal of neuropathology and experimental neurology 1990;49(2):137-49.
1990: Hans H Goebel; J Bohl; S Störkel
Amyloid-related neuropathies.
Zentralblatt für allgemeine Pathologie und pathologische Anatomie 1990;136(6):517-23.
1990: Hans H Goebel
Hereditary metabolic neuropathies.
Zentralblatt für allgemeine Pathologie und pathologische Anatomie 1990;136(6):503-15.
1989: Hans H Goebel
Diagnostic morphology of human eye-related storage disorders.
Ophthalmic paediatrics and genetics 1989;10(3):199-209.
1989: Hans H Goebel; Heiko Braak
Adult neuronal ceroid-lipofuscinosis.
Clinical neuropathology 1989;8(3):109-19.
1989: Hans H Goebel; A Bornemann; Heinz Reichmann
Mitochondria-related encephalomyopathies.
Neuropathology and applied neurobiology 1989;15(2):97-119.
1989: U Kaesgen; Hans H Goebel
Intraepidermal morphologic manifestations in lysosomal diseases.
Brain & development 1989;11(5):338-41.
1989: Hans H Goebel; G Stolte; B Kustermann-Kuhn; Klaus Harzer
B1 variant of GM2 gangliosidosis in a 12-year-old patient.
Pediatric research 1989;25(1):89-93.
1989: Hans H Goebel; H Busch
Abnormal lipopigments and lysosomal residual bodies in metachromatic leukodystrophy.
Advances in experimental medicine and biology 1989;266():299-309.
1988: Hans H Goebel; H Klein; P Santavuori; K Sainio
Ultrastructural studies of the retina in infantile neuronal ceroid-lipofuscinosis.
Retina (Philadelphia, Pa.) 1988;8(1):59-66.
1988: L Halbig; L Gutmann; Hans H Goebel; J F Brick; S Schochet
Ultrastructural pathology in emetine-induced myopathy.
Acta neuropathologica 1988;75(6):577-82.
1988: Hans H Goebel; R Besser
Traumatic fascicular neuroma.
Acta neuropathologica 1988;75(3):321-4.
1988: A Bornemann; Manfred Schwarz; K Brühl; Hans H Goebel
A sphenoorbital encephalocele--clinical, radiological, and morphological findings.
Neurosurgical review 1988;11(2):205-6.
1988: S Walter; Hans H Goebel
Ultrastructural pathology of dermal axons and Schwann cells in lysosomal diseases.
Acta neuropathologica 1988;76(5):489-95.
1988: Hans H Goebel; Thomas Bilzer; E Dahme; F Malkusch
Morphological studies in canine (Dalmatian) neuronal ceroid-lipofuscinosis.
American journal of medical genetics. Supplement 1988;5():127-39.
1987: Hans H Goebel; A Bardosi
Myoadenylate deaminase deficiency.
Klinische Wochenschrift 1987;65(21):1023-33.
1987: S Kimura; Hans H Goebel
Electron microscopic studies on skin and lymphocytes in early juvenile neuronal ceroid-lipofuscinosis.
Brain & development 1987;9(6):576-80.