M. Bruyland

发表

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

C. van Broeckhoven, J. Collinge, P. Johannsen, 2010, Human molecular genetics.

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

F. Jessen, G. Frisoni, B. Bergmans, 2017, Human mutation.

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

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

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

Patrick Santens, Karin Peeters, Rik Vandenberghe, 2008, Human molecular genetics.

Pleocore disease

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

Dynamic training of skeletal muscle ventricles. A method to increase muscular power for cardiac assistance.

H. Eichstaedt, E. Wyffels, V. Umbrain, 1994, Circulation.

Non-traumatic subdural hygroma.

T. Stadnik, R. Dierckx, G. Ebinger, 1989, Acta neurologica Belgica.

Osteopathia striata with cranial sclerosis Report of a case and review of the literature

J. Keyser, J. Leemans, G. Ebinger, 1983, Clinical Neurology and Neurosurgery.

Letters to the editor: Letters to the Editor

N. Chu, Chin‐Chang Huang, J. Slopis, 1991 .

FLEXION CONTRACTURES: A FORGOTTEN SYMPTOM IN ADDISON'S DISEASE AND HYPOPITUITARISM

G. Somers, G. Ebinger, R. Six, 1986, The Lancet.

Monoaminergic neurotransmitters in Alzheimer's disease An HPLC study comparing presenile familial and sporadic senile cases

Y. Michotte, J. Keyser, G. Ebinger, 1989, Journal of 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.

Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families

C. Broeckhoven, H. Backhovens, A. Wehnert, 1987, Nature.

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.

Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3

C. Broeckhoven, M. Cruts, H. Backhovens, 1992, Nature Genetics.

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

B. Bergmans, C. Broeckhoven, S. Engelborghs, 2017, Neurobiology of Aging.

Lower motor neuron disease in a patient with hodgkin's disease treated with radiotherapy

G. Storme, J. Keyser, G. Ebinger, 1984, Clinical Neurology and Neurosurgery.

Genetic Linkage Analysis in Early-Onset Familial Alzheimer’s Dementia

C. Broeckhoven, H. Backhovens, A. Wehnert, 1990 .

Cyclosporine and myopathy.

M. Noppen, L. Vanhaelst, B. Velkeniers, 1987, Annals of internal medicine.

Recurrent forms of sporadic brachial plexus neuropathy A report of two cases

A. Michotte, R. Dierckx, D. Deleu, 1988, Clinical Neurology and Neurosurgery.

Muscular fibrosis due to chronic intramuscular administration of narcotic analgesics.

D. Deleu, K. von Kemp, P. Herregodts, 1989, Acta clinica Belgica.

Two novel mutations of the porphobilinogen deaminase gene in acute intermittent porphyria.

F. D. de Rooij, B. Grandchamp, W. Lissens, 1993, Human molecular genetics.

Fascial Tc-99m MDP uptake in eosinophilic fasciitis as demonstrated by SPECT.

P. Flamen, A. Bossuyt, P. Franken, 1997, Clinical nuclear medicine.

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder

I. Rainero, J. L. Haines, J. A. Hardy, 1990, Nature.

Idiopathic hemiparetic parkinsonism, a syndrome distinct from idiopathic parkinsonism

J. Keyser, G. Ebinger, L. Herroelen, 1992, The Lancet.

Sudden hearing loss and facial palsy at the contralateral side following acoustic tumour removal.

J. De Keyser, G. Ebinger, M. Bruyland, 1983, Journal of neurology, neurosurgery, and psychiatry.

Osteomalacia in a patient with anorexia nervosa.

M. Shahabpour, L. Verbruggen, M. Bruyland, 1993, The Journal of rheumatology.

An unusual cause of attacks of focal cerebral symptoms: Multiple endocrine neoplasia type IIa

G. Ebinger, R. Six, L. Verbruggen, 1983, Clinical Neurology and Neurosurgery.