J. Martin

发表

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement

C. Broeckhoven, C. van Broeckhoven, J. Martín, 2004, Neurology.

Distribution of biogenic amines and their catabolites in brains from patients with Alzheimer's disease

Y. Michotte, J. Martín, P. Cras, 1987, Journal of the Neurological Sciences.

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.

Multiple system atrophies. A neuropathological and neurochemical study.

J. Martín, W. Dierick, G. V. Van Dessel, 1974, Journal of the neurological sciences.

Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.

J. Lupski, C. van Broeckhoven, J. Martín, 1997, Journal of medical genetics.

Skin and conjunctival biopsies in adrenoleukodystrophy

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

Postmortem MRI of the brain with neuropathological correlation

P. M. Parizel, P. Deyn, P. Parizel, 1995, Neuroradiology.

In vitro contracture tests in patients with various neuromuscular diseases.

L. Bossaert, J. Martín, L. Heytens, 1992, British journal of anaesthesia.

A prospective study of CSF markers in 250 patients with possible Creutzfeldt–Jakob disease

J. Martín, P. Cras, S. Quoilin, 2003, Journal of neurology, neurosurgery, and psychiatry.

The many faces of human prion diseases in Belgium and the world.

J. Martín, S. Quoilin, B. V. Van Everbroeck, 2001, Acta neurologica Belgica.

Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings

J. Martín, P. Cras, R. Dom, 2000, Acta Neuropathologica.

ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families.

J. Hardy, M. Rossor, C. van Broeckhoven, 1998, American journal of medical genetics.

Encephalitis with myoclonus in Whipple's disease.

J. Martín, R. Heimann, G. Monseu, 1969, Journal of neurology, neurosurgery, and psychiatry.

Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy.

C. van Broeckhoven, J. Martín, B. Ceulemans, 2001, Pathology, research and practice.

Niemann-Pick disease (Crocker's group A). Late onset and pigmentary degeneration resembling Hallervorden-Spatz syndrome.

J. Martín, J. Callahan, M. Philippart, 1972, Archives of neurology.

Glycolipid alterations in Niemann-Pick disease (Crocker type C).

M. Philippart, L. Martin, J. Martin, 1968, 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.

I-Cell disease (Mucolipidosis II)

J. Martín, R. Desnick, J. Leroy, 1975, Acta Neuropathologica.

Muscle carnitine deficiency in old age Case report and therapeutic results

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

ANTECOLLIS IN PARKINSONISM

J. Martín, P. Jorens, G. Parizel, 1989, The Lancet.

A new combined Bodian-Luxol technique for staining unmyelinated axons in semithin, resin-embedded peripheral nerves: a comparison with electron microscopy

J. Martín, A. Fumal, M. Deprez, 1999, Acta Neuropathologica.

Adrenomyeloneuropathy

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

Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency

J. Martín, B. Berra, R. Gatti, 1982, Journal of Inherited Metabolic Disease.

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

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

Niemann-Pick disease. Morphologic and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C).

J. Martín, M. Philippart, J. Menkes, 1969, Archives of neurology.

Pompe's disease: An inborn lysosomal disorder with storage of glycogen

J. Martín, F. Hoof, G. Palladini, 1973, Acta Neuropathologica.

Skin biopsy as a contribution to diagnosis in late infantile amaurotic idiocy with curvilinear bodies.

J. Martín, K. Jacobs, J. Martin, 1973, European neurology.

Hereditary pressure-sensitive neuropathy

J. Martín, I. Dehaene, J. Debruyne, 1980, Journal of the Neurological Sciences.

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

F. Baas, C. Broeckhoven, J. Martín, 1991, Neuromuscular Disorders.

Acid maltase deficiency (Type II glycogenosis) Morphological and biochemical study of a childhood phenotype

J. Martín, G. Palladini, J. Leroy, 1976, Journal of the Neurological Sciences.

Menkes kinky-hair disease. A report on its pathology

J. Martín, N. Buyssens, J. Flament-Durand, 1978, Acta Neuropathologica.

Analysis of the prion protein gene in thalamic dementia

J. Martín, R. Petersen, W. Pendlebury, 1992, Neurology.

Schilder's diffuse sclerosis.

J. Martín, G. Guazzi, J. Martin, 1991, Developmental neuroscience.

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.

[On a status marmoratus with thalamic predilection and pseudosystemic localization. (Its differentiation from primary degenerations)].

H. Ishino, T. Masini, J. Martin, 1967, 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.

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 .