C. Ceuterick

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Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies

J. Meuleman, K. Venken, V. Timmerman, 2001, Neuroreport.

Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase.

J. Martín, H. Scholte, C. Ceuterick, 1986, Neuropediatrics.

Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia

J. Martín, H. Scholte, C. Ceuterick, 1988, Journal of the Neurological Sciences.

Adrenomyeloneuropathy. A report on two families.

J. Martín, A. Lowenthal, C. Ceuterick, 1982, Journal of neurology.

Adrenomyeloneuropathy and adrenoleukodystrophy in two brothers.

J. Martín, C. Ceuterick, K. Jacobs, 1980, European neurology.

Skin and conjunctival biopsies in adrenoleukodystrophy

J. Martín, C. Ceuterick, L. Martin, 1977, Acta Neuropathologica.

Skin and conjunctival nerve biopsies in adrenoleukodystrophy and its variants

J. Martín, C. Ceuterick, J. Libert, 1980, Annals of neurology.

Morphological study of skin biopsy specimens: a contribution to the diagnosis of metabolic disorders with involvement of the nervous system.

J. Martín, C. Ceuterick, J. Martín, 1978, Journal of neurology, neurosurgery, and psychiatry.

Early‐onset Alzheimer's disease in 2 large Belgian families

C. van Broeckhoven, J. Martín, P. Cras, 1991, Neurology.

Type I Sialidosis: A Clinical, Biochemical and Neuroradiological Study

G. Guazzi, A. Malandrini, M. Villanova, 2000, European Neurology.

Infantile and juvenile presentations of Alexander's disease: a report of two cases

J. Martín, L. Leval, M. Deprez, 1999, Acta neurologica Scandinavica.

Juvenile dystonic lipidosis (variant of Niemann-Pick disease type C)

J. Martín, A. Lowenthal, M. Vanier, 1984, Journal of the Neurological Sciences.

Neuropathology of some hereditary conditions affecting central and peripheral nervous system.

J. Martín, C. Ceuterick, J. Martín, 2002, Acta neurologica Belgica.

Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease.

J. Lupski, C. Boerkoel, L. Potocki, 2003, Brain : a journal of neurology.

Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24.

C. van Broeckhoven, J. Martín, J. Beuten, 1996, Human molecular genetics.

A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

J. Meuleman, J. Martín, C. Broeckhoven, 2001, Neuromuscular Disorders.

Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype

J. Lupski, C. van Broeckhoven, V. Timmerman, 1999, Neurology.

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.

C. van Broeckhoven, J. Martín, V. Timmerman, 1999, Brain : a journal of neurology.

G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy

S. Züchner, K. Claeys, J. Martín, 2006, Neuromuscular Disorders.

Mutations in GDAP1

C. van Broeckhoven, F. Palau, V. Timmerman, 2002, Neurology.

Becker-type muscular dystrophy Report of a family with one postmortem study

C. Broeckhoven, C. Ceuterick, U. Lübke, 1992, Clinical Neurology and Neurosurgery.

Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692 Ala → Gly mutation

A. Hofman, C. Broeckhoven, L. Hendriks, 1998 .

[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].

J. Meuleman, J. Martín, V. Timmerman, 2002, Revue neurologique.

Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy

C. van Broeckhoven, F. Palau, V. Timmerman, 2002 .

Pleocore disease

J. Martín, H. Busch, C. Ceuterick, 2004, Acta Neuropathologica.

Specific monoclonal antibodies against normal microtubule-associated protein-2 (MAP2) epitopes present in Alzheimer pathological structures do not recognize paired helical filaments

M. Vandermeeren, M. Mercken, J. Six, 2004, Acta Neuropathologica.

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

C. Broeckhoven, J. Martín, J. Brucher, 2004, Acta Neuropathologica.

Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disorders.

M. Vandermeeren, J. Six, J. Martín, 1994, The American journal of pathology.

Sanfilippo A disease in the fetus--comparison with pre- and postnatal cases.

J. Martín, C. Ceuterick, J. Libert, 1980, Neuropadiatrie.

Two cases of mucopolysaccharidosis Type III (Sanfilippo) A biochemical study

J. Martín, W. Dierick, C. Ceuterick, 1979, Journal of the Neurological Sciences.

The contribution of pathology to the study of storage disorders.

J. Martín, C. Ceuterick, 1988, Pathology, research and practice.

Nuclear inclusions in oculopharyngeal muscular dystrophy

R. Mercelis, C. Ceuterick, Jean‐Jacques R. Martin, 1982 .

Hyaline bodies in skeletal muscle of a patient with a mild chronic nonprogressive congenital myopathy.

J. Martín, C. Ceuterick, C. Martens, 1993, Clinical neuropathology.

Electron microscopic features of skin in neurometabolic disorders

C. Ceuterick, J. Martin, 1992, Journal of the Neurological Sciences.

Adult ceroid-lipofuscinosis: diagnostic value of biopsies and of neurophysiological investigations.

J. Martín, C. Ceuterick, A. Vercruyssen, 1982, Journal of neurology, neurosurgery, and psychiatry.

The Diagnosis of Infantile Generalized Ceroid-Lipofuscinosis (Type Hagberg-Santavuori) Using Skin Biopsy

J. Martín, P. Casaer, C. Ceuterick, 1976, Neuropadiatrie.

Fetal Krabbe leukodystrophy

J. Martín, C. Ceuterick, J. Leroy, 2004, Acta Neuropathologica.

Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)

J. Martín, G. Guazzi, A. Malandrini, 1999, Acta Neuropathologica.

Nerve biopsy findings in Niemann-Pick type II (NPC)

J. Martín, A. Hahn, C. Ceuterick, 2004, Acta Neuropathologica.

Krabbe globoid cell leukodystrophy. Electron microscopy shows characteristic inclusions in eccrine sweat glands.

J. Martín, C. Ceuterick, 1993, Pathology, research and practice.

I-cell disease

J. Martín, C. Ceuterick, J. Leroy, 1984, Acta Neuropathologica.

Acid maltase deficiency in adults. A study of five cases.

T. de Barsy, J. J. Martin, C. Ceuterick, 1986, Acta neurologica Belgica.

Niemann-Pick disease type C. Skin biopsies in parents.

J. Martín, M. Foulard, C. Ceuterick, 1986, Neuropediatrics.

Encephalopathy associated with lamellar residual bodies in astrocytes (Towfighi, Grover and Gonatas 1975):a new observation.

J. Martín, C. Ceuterick, L. Martin, 1977, Neuropadiatrie.

[Skin biopsy in the diagnosis of metabolic encephalopathies].

J. Martín, C. Ceuterick, J. Leroy, 1976, Revue neurologique.

Adult ceroid-lipofuscinosis (Kufs' disease) in two brothers. Retinal and visceral storage in one; Diagnostic muscle biopsy in the other

J. Martín, R. Dom, J. Brucher, 1979, Acta Neuropathologica.

Carbohydrate‐deficient glycoprotein syndrome with previously unreported features

F. Eyskens, J. Jaeken, J. Jaeken, 1994, Acta paediatrica.

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

C. Broeckhoven, J. Martín, B. Dermaut, 2003, Neuromuscular Disorders.

Unusual presentation and clinical variability in Belgian pedigrees with progressive external ophthalmoplegia and multiple deletions of mitochondrial DNA

C. Broeckhoven, I. Dehaene, C. Broeckhoven, 1997 .

Cerebral cysticercosis. Light- and electron microscopy report on one case.

J. Martín, P. de Jonghe, C. Ceuterick, 1980, Annales de la Societe belge de medecine tropicale.

Intermediate syndrome due to prolonged parathion poisoning

J. Reuck, D. Vogelaers, C. Ceuterick, 1992, Acta neurologica Scandinavica.

Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs.

J. Martín, R. Mercelis, C. Ceuterick, 1980, Acta neurologica Belgica.

[Centronuclear myopathy (author's transl)].

J. Martín, C. Ceuterick, C. Martens, 1977, Acta neurologica Belgica.

A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.

C. van Broeckhoven, J. Martín, V. Timmerman, 1999, Archives of neurology.

Patient homozygous for a recessive POLG mutation presents with features of MERRF

S. Seneca, C. van Broeckhoven, J. Martín, 2003, Neurology.

Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody.

C. van Broeckhoven, J. Del-Favero, C. Ceuterick, 1999, Brain research. Molecular brain research.

Two cases of mucopolysaccharidosis type III (Sanfilippo)

J. Martín, W. Dierick, C. Ceuterick, 1979, Acta Neuropathologica.

Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases.

J. Martín, C. Ceuterick, J. Martín, 1983, Clinical neuropathology.

Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation

A. Hofman, C. Broeckhoven, C. van Broeckhoven, 1998, Acta Neuropathologica.

LEIGH'S DISEASE ‐SEVERAL NOSOLOGICAL ENTITIES WITH AN IDENTICAL HISTOPATHOLOGICAL COMPLEX?

J. Martín, J. Brucher, C. Ceuterick, 1986, Neuropathology and applied neurobiology.

Familial periodic paralysis with hypokalaemia. Study of a muscle biopsy in the myopathic stage of the disorder.

J. Martín, D. Amrom, R. Mercelis, 1984, Acta neurologica Belgica.

Cerebral manifestations of Whipple's disease.

H. Budka, J. Martín, P. de Jonghe, 1979, Acta neurologica Belgica.

Chronic colchicine-induced myopathy and neuropathy.

J. Martín, C. Ceuterick, R. Crols, 1995, Acta neurologica Belgica.

Is congenital fibre type disproportion a true myopathy?

J. Martín, C. Ceuterick, R. Clara, 1976, Acta neurologica Belgica.

Muscle carnitine deficiency in old age Case report and therapeutic results

J. Martín, C. Ceuterick, A. Vercruyssen, 1985, Clinical Neurology and Neurosurgery.

Astroglial tangles in the hippocampus of two patients with Down syndrome and Alzheimer neuropathology.

J. Martín, P. Cras, C. Ceuterick, 1998, Ultrastructural pathology.

The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case.

J. Martín, C. Ceuterick, J. Leroy, 1984, Neuropediatrics.

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

G. Guazzi, A. Malandrini, M. Villanova, 2001, Journal of submicroscopic cytology and pathology.

Ocular ultrastructural study in a fetus with type II glycogenosis.

C. Ceuterick, P. Danis, J. Libert, 1977, The British journal of ophthalmology.

Adrenomyeloneuropathy

A. Lowenthal, C. Ceuterick, W. Dickey, 2004, Journal of Neurology.

Autosomal recessive inheritance of polymicrogyria and dermatomyositis with paracrystalline inclusions.

J. D. Reuck, C. Ceuterick, J. Martin, 1990, Clinical neuropathology.