J. Martín

发表

Detection of tau proteins in normal and Alzheimer's disease cerebrospinal fluid with a sensitive sandwich enzyme-linked immunosorbent assay.

M. Vandermeeren, M. Mercken, E. Vanmechelen, 1993, Journal of neurochemistry.

Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis.

C. van Broeckhoven, J. Martín, E. Nelis, 1993, Human molecular genetics.

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.

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.

Hereditary neuromuscular diseases.

P. Parizel, J. V. Van Goethem, Ö. Özşarlak, 2001, European journal of radiology.

[Susac syndrome: clinical and diagnostic approach. A new case report].

J. Martín, J. Meca-Lallana, J. Marín, 1999, Revista de neurologia.

Detection of herpes simplex virus in the cerebrospinal fluid of patients with encephalitis using the polymerase chain reaction

P. Parizel, J. Martín, M. Ieven, 1993, Journal of the Neurological Sciences.

Cerebral ganglioglioma and neurofibromatosis type I

P. Parizel, J. Martín, L. Hauwe, 1991, Neuroradiology.

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.

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

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

High resolution nuclear magnetic resonance imaging of the spinal cord in experimental demyelinating disease

A. Connelly, J. Martín, J. Gheuens, 2004, Acta Neuropathologica.

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.

Neuropathology of peroxisomal diseases

J. Martín, J. J. Martín, 1995, Journal of Inherited Metabolic Disease.

Skin and conjunctival biopsies in adrenoleukodystrophy

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

Neurophysiological studies in adrenomyeloneuropathy A report on five cases

J. Martín, R. Mercelis, A. Vercruyssen, 1982, Journal of the Neurological Sciences.

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.

ANTECOLLIS IN PARKINSONISM

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

Spinocerebellar degeneration

J. Martín, J. Oonk, H. J. van der Helm, 1979, Neurology.

Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

C. van Broeckhoven, J. Martín, V. Timmerman, 1990, American journal of human genetics.

Idiopathic orthostatic hypotension and the Shy and Drager syndrome; Physiological studies in four cases; pathological report of one case.

L. Bossaert, J. Martín, J. Snoeck, 1977, Acta cardiologica.

Beta-amyloid precursor protein and early-onset Alzheimer's disease.

C. Broeckhoven, L. Hendriks, J. Martín, 1996, Ciba Foundation symposium.

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

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

Acoustic schwannoma: MR findings in 84 tumors.

P. Parizel, T. Mulkens, P. van de Heyning, 1993, AJR. American journal of roentgenology.

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

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

[Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction].

A. Destée, A. Verier, J. Martín, 1989, Revue neurologique.

Primary intracerebral lymphoma in systemic lupus erythematosus treated with immunosuppressives.

J. Martín, P. Cras, C. Franckx, 1989, Clinical neuropathology.

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

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

Metrizamide myelography combined with computed tomography in adrenomyeloneuropathy.

J. Martín, K. Jacobs, J. de Moor, 1982, Archives of neurology.

Distal hereditary motor neuropathy type II (distal HMN type II): phenotype and molecular genetics.

C. van Broeckhoven, J. Martín, J. Beuten, 1999, Annals of the New York Academy of Sciences.

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.

Peripheral myelin protein‐22 expression in charcot‐marie‐tooth disease type 1a sural nerve biopsies

C. van Broeckhoven, J. Martín, G. Stoll, 1994, Journal of neuroscience research.

Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease

C. van Broeckhoven, J. Martín, H. Houlden, 2006 .

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.

Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP.

P. Patel, C. van Broeckhoven, J. Martín, 1998, Journal of medical genetics.

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

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

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.

Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3.

J. Weissenbach, D. Le Paslier, A. Goate, 1995, Human molecular genetics.

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.

Guillain‐Barré syndrome with ophthalmoplegia

J. Martín, P. Cras, I. Dehaene, 1986, Neurology.

Magnetic resonance imaging in the evaluation of patients with eosinophilic fasciitis.

A. D. De Schepper, J. Martín, W. Stevens, 1989, The Journal of rheumatology.

Adult type of neuronal ceroid-lipofuscinosis

J. Martín, 1993, Journal of Inherited Metabolic Disease.

Adult type of neuronal ceroid lipofuscinosis.

J. Martín, 1991, Developmental neuroscience.

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 .

Selective thalamic degeneration--report of a case with memory and mental disturbances.

J. Martín, M. Yap, I. Nei, 1983, Clinical neuropathology.

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

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

Neuroradiologic findings in leptomeningeal carcinomatosis: the value interest of gadolinium-enhanced MRI

P. Parizel, C. Segebarth, J. Martín, 2004, Neuroradiology.

Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.

J. Martín, F. Meire, R. Van Coster, 1995, Ophthalmic genetics.

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.

Long term follow-up of multiple sclerosis by standardized, non-contrast-enhanced magnetic resonance imaging

P. Parizel, J. Martín, L. Truyen, 1991, Journal of the Neurological Sciences.

Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency

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

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.

A family with different clinical forms of acid maltase deficiency (glycogenosis type 11)

J. Martín, J. Tager, M. Niermeijer, 1981, Neurology.

Sensitivity and specificity of thallium-201 single-photon emission tomography in the functional detection and differential diagnosis of brain tumours

J. Martín, R. Dierckx, A. Dobbeleir, 1994, European Journal of Nuclear Medicine.

γ-Enolase and glial fibrillary acidic protein in nervous system tumors

J. Martín, P. Cras, J. Gheuens, 1988, Acta Neuropathologica.

Gamma-enolase and glial fibrillary acidic protein in nervous system tumors. An immunohistochemical study using specific monoclonal antibodies.

J. Martín, P. Cras, J. Gheuens, 1988, Acta neuropathologica.

Nerve biopsy: indications and contribution to the diagnosis of peripheral neuropathy. The experience of the Born Bunge Foundation University of Antwerp and University of Liege between 1987 and 1997.

J. Schoenen, J. Martín, M. Deprez, 2000, Acta neurologica Belgica.

Cardiac manifestations of Becker-type muscular dystrophy.

J. Martín, R. Mercelis, C. Vrints, 1983, Acta cardiologica.

Transmission and age-at-onset patterns in familial Alzheimer??s disease: evidence for heterogeneity

J. Growdon, M. Rossor, L. Farrer, 1991 .

Pleocore disease

J. Martín, H. Busch, C. Ceuterick, 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.

Eosinophilia myalgia syndrome: absence of immunoglobulin reactivity suggests a cellular rather than humoral mechanism.

J. Martín, P. Cras, G. Guazzi, 1994, Acta neurologica Belgica.

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.

Menkes kinky-hair disease. A report on its pathology

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

Laing early-onset distal myopathy in a Belgian family

J. Martín, P. Bergh, F. Lecouvet, 2014, Acta Neurologica Belgica.

Primary thalamic malignant fibrous histiocytoma of the dominant hemisphere causing severe neuropsychological symptoms.

P. Paquier, J. Martín, P. Cras, 1989, Clinical neuropathology.

Multiple pterygium syndrome with body asymmetry.

E. van Marck, P. Parizel, C. Colpaert, 1993, American journal of medical genetics.

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

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

Encephalitis with myoclonus in Whipple's disease.

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

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

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

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.

Identification of heterozygotes for glycogenosis 2 (Acid maltase deficiency)

J. Martín, J. Tager, M. Niermeijer, 1981, Clinical genetics.

Transient musical hallucinosis of central origin: a review and clinical study.

P. Parizel, P. Paquier, J. Martín, 1992, Journal of neurology, neurosurgery, and psychiatry.

Diagnosis of bilateral hydronephrosis in utero by ultrasonography.

E. Taylor, J. Martín, 1981, Urology.

Intracerebral hemorrhage due to cerebral amyloid angiopathy. Case report.

J. Martín, N. Roosen, C. De La Porte, 1985, Journal of neurosurgery.

Infantile Neuroaxonal Dystrophy

J. Martín, L. Martin, 1972 .

Infantile neuroaxonal dystrophy. Ultrastructural study of the peripheral nerves and of the motor end plates.

J. Martín, L. Martin, 1972, European neurology.

Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.

J. Martín, J. Leroy, C. Navarro, 1973, The New England journal of medicine.

The contribution of pathology to the study of storage disorders.

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

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

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

Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits.

P. Munroe, F. Andermann, Y. Crow, 1998, Human molecular genetics.

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.

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

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

In vitro diagnosis of malignant hyperthermia: influence of electrical stimulation on the contracture response to caffeine.

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

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.

A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities.

J. Martín, I. Buntinx, J. Dumon, 1991, Genetic counseling.

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.

Skin biopsy is useful for diagnosis of infantile neuroaxonal dystrophy

J. Martín, C. Ceuterick PhD, 1990, Annals of neurology.

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.

Peroxidase in ceroid-lipofuscinosis

J. Martín, W. D. Tandt, 1978, Journal of the Neurological Sciences.

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.

Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant.

J. Martín, A. Yoshida, P. Willems, 1996, Archives of biochemistry and biophysics.

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

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

Loss of constitutional heterozygosity in human astrocytomas

J. Martín, P. Willems, P. Selosse, 2005, Acta Neurochirurgica.

Instability of microsatellites in human gliomas.

J. Martín, E. Dams, P. Willems, 1995, Cancer research.

SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I

J. Martín, K. Verhoeven, V. Timmerman, 2004, Neurology.

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.

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement

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

Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA

C. van Broeckhoven, J. Martín, A. Löfgren, 2000, Journal of medical genetics.

Atypical clinical presentation of ataxia telangiectasia.

J. Martín, P. Willems, W. Kleijer, 1993, American journal of medical genetics.

Acid maltase deficiency in non-identical adult twins

J. Martín, W. D. Tandt, T. Barsy, 1976, Journal of Neurology.

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

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

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.

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.

Oculopharyngeal muscular dystrophy (OPMD)

C. C. Tijssen, B. Brais, J. Martín, 1997 .

In vitro contracture tests in patients with various neuromuscular diseases.

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

Clinical and neuropathological parameters affecting the diagnostic yield of nerve biopsy

J. Martín, L. Gollogly, M. Deprez, 2000, Neuromuscular Disorders.

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.

On some myopathies with oculomotor involvement.

J. Martín, 1987, Acta neurologica Belgica.

Neonatal myotubular myopathy with a probable X-linked inheritance: observations on a new family with a review of the literature

J. Martín, I. Liebaers, L. Meirleir, 2004, Journal of Neurology.

Cardiac involvement in juvenile ceroid lipofuscinosis of the Spielmeyer-Vogt-Sjögren type: prospective noninvasive findings in two siblings.

J. Martín, T. Gillebert, P. Michielsen, 1984, European neurology.

Multiple system atrophies. A neuropathological and neurochemical study.

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

Wolman's disease.

J. Martín, G. Guazzi, H. Roels, 1968, European neurology.

Tuberculous meningitis in immunocompetent adults: two cases with a clinico-radiological discussion

J. Martín, L. Truyen, A. Vercruyssen, 1996, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

C. van Broeckhoven, J. Martín, W. Hul, 1992, Journal of medical genetics.

Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

C. van Broeckhoven, J. Martín, V. Timmerman, 1989, American journal of human genetics.

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.

Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.

C. van Broeckhoven, J. Martín, D. Fitzpatrick, 1997, Journal of neurology, neurosurgery, and psychiatry.

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

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

Familial erythrophagocytic lymphohistiocytosis

J. Martín, P. Cras, 1985, Acta Neuropathologica.

Hereditary pressure-sensitive neuropathy

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

Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.

J. Martín, L. Messiaen, E. Vamos, 1998, American journal of medical genetics.

I-Cell disease (Mucolipidosis II)

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

Wolman's disease. Distribution and significance of the central nervous system lesions.

J. Martín, G. Guazzi, H. Roels, 1968, Pathologia Europaea.

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

J. Theuns, H. Backhovens, A. Wehnert, 1998, Human molecular genetics.

Charcot Joint in Idiopathic Sensorimotor Neuropathy

J. Martín, J. Willems, R. Chappel, 2000, Clinical Rheumatology.

Two cases of mucopolysaccharidosis type III (Sanfilippo)

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

Sellar metastatic disease

J. Bultinck, J. Martín, A. Neetens, 1982 .

Transient global amnesia following ingestion of chloroquine.

J. Martín, P. Cras, 1990, Journal of neurology, neurosurgery, and psychiatry.

Intrasellar adenoma and chordoma

J. Martín, A. Neetens, J. Solheid, 1980 .

Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases.

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

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

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

Coma as a presenting sign of Epstein-Barr encephalitis.

L. Bossaert, J. Martín, H. Demey, 1988, Archives of internal medicine.

Analysis of the prion protein gene in thalamic dementia

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

Neuropathology of citrullinaemia

J. Martín, P. Jonghe, J. Farriaux, 2004, Acta Neuropathologica.

The hereditary familial optic atrophies

J. Martín, A. Neetens, J. Martín, 1986 .

[The adult form of Leigh's necrotizing encephalopathy with chronic evolution. Its comparison with the infantile and juvenile forms].

J. Martín, C. Solheid, N. Stoupel, 1971, Acta neurologica Belgica.

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.

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.

Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

C. van Broeckhoven, J. Martín, V. Timmerman, 1994, Journal of medical genetics.

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.

Myoadenylate deaminase deficiency in a patient with facial and limb girdle myopathy

J. Martín, I. Dehaene, R. Mercelis, 2004, Journal of Neurology.

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.

[Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects].

J. Martín, J. Radermecker, M. Jj, 1972, Bulletin de l'Academie royale de medecine de Belgique.

The association of meningioma and pituitary adenoma: report of seven cases and review of the literature.

E. van Marck, P. Parizel, J. Martín, 1993, European neurology.

Laing early-onset distal myopathy in a Belgian family

J. Martín, P. Bergh, F. Lecouvet, 2014, Acta Neurologica Belgica.

Haemodynamically unstable pulmonary embolism in the RIETE Registry: systolic blood pressure or shock index?

J. Martín, R. Otero, M. Monreal, 2007, European Respiratory Journal.

Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium

J. Martín, P. Cras, C. Godfraind, 2006, European Journal of Epidemiology.

Is congenital fibre type disproportion a true myopathy?

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

Infantile form of meningeal angiomatosis with sudanophilic leucodystrophy associated with complex abiotrophies. Study of a second family.

J. Martín, G. Guazzi, J. Bruens, 1968, Journal of the neurological sciences.

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.

M. Cruts, J. Martín, P. Cras, 2001, Brain : a journal of neurology.

Patterns of disease activity in multiple sclerosis.

J. Martín, L. Truyen, J. Gheuens, 1990, BMJ.

Spinal neuroaxonal dystrophy and angioneuromatosis

E. Schutter, J. Martín, P. Cras, 2004, Acta Neuropathologica.

Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency.

J. Six, J. Martín, G. Guazzi, 1996, Journal of submicroscopic cytology and pathology.

Muscle carnitine deficiency in old age Case report and therapeutic results

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

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

C. Broeckhoven, C. van Broeckhoven, A. Dürr, 2001, Brain : a journal of neurology.

Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.

W. Schlote, J. Martín, 1972, Journal of the neurological sciences.

Postmortem MRI of the brain with neuropathological correlation

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

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

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

Improved sensitivity of MRI in multiple sclerosis by use of extensive standardized procedures.

J. Martín, L. Truyen, Jean-Jacques Martin, 1989, Magnetic resonance imaging.

Infantile form of Hallervorden-Spatz disease

J. Martín, L. Martin, 1974 .

Postmortem examination of two fragile X brothers with an FMR1 full mutation.

E. van Marck, B. Oostra, J. Martín, 1999, American journal of medical genetics.

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

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

Bismuth encephalopathy. A clinical and anatomo-pathological report of one case.

J. Martín, J. Liessens, J. Monstrey, 1978, Acta neurologica Belgica.

Functional anatomy, vascularisation and pathology of the human thalamus.

S. Engelborghs, P. Mariën, J. Martín, 1998, Acta neurologica Belgica.

Comparative Neuropathology of Subacute Sclerosing Panencephalitis

J. Martín, J. Martín, 1979 .

Disturbed vertical optokinetic nystagmus: Possible sign of striato-nigral pathway involvement

H. Smet, J. Martín, P. V. D. Ende, 1991 .

Perfusion and thallium single photon emission computed tomography in herpes simplex encephalitis

J. Martín, B. Pickut, P. Deyn, 1998, Journal of Neurological Sciences.

Skin and conjunctival biopsies in infantile neuroaxonal dystrophy

J. Martín, J. Leroy, M. Eygen, 1979, Acta Neuropathologica.

Whole-body MR screening of muscles in the evaluation of neuromuscular diseases

P. Parizel, Ö. Özşarlak, A. D. De Schepper, 2004, European Radiology.

"Locked-in" syndrome. A clinico-pathological study of two cases.

J. Martín, I. Dehaene, 1976, European neurology.

Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits.

F. Andermann, J. Martín, E. Andermann, 1997, Neuropediatrics.

Schilder's diffuse sclerosis.

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