Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("VAN DAMME, Philip")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 22 of 22

  • Page / 1
Export

Selection :

  • and

Essay nomaVAN DAMME, Philip A.Lancet (British edition). 2006, Vol 368, issn 0140-6736, S61-S62, NSArticle

An unusual presentation of Guillain—Barré syndrome associated with monospecific anti-GD1b antibodiesDEWIL, Maarten; ROBBERECHT, Wim; VAN DAMME, Philip et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 5, pp 587-588, issn 0022-3050, 2 p.Article

Autosomal recessive spastic ataxia of Charlevoix-SaguenayVAN DAMME, Philip; DEMAEREL, Philippe; SPILEERS, Werner et al.Neurology. 2009, Vol 72, Num 20, issn 0028-3878, p. 1790Article

The transconjunctival approach with lateral canthal extension for three-wall orbital decompression in thyroid orbitopathyBARKHUYSEN, Richard; NIELSEN, Chris C. M; KLEVERING, B. Jeroen et al.Journal of cranio-maxillo-facial surgery. 2009, Vol 37, Num 3, pp 127-131, issn 1010-5182, 5 p.Article

The AMPA receptor antagonist NBQX prolongs survival in a transgenic mouse model of amyotrophic lateral sclerosisVAN DAMME, Philip; LEYSSEN, Maarten; CALLEWAERT, Geert et al.Neuroscience letters. 2003, Vol 343, Num 2, pp 81-84, issn 0304-3940, 4 p.Article

Normalization of 14-3-3 in CJDSCHROOTEN, Maarten; DE VOOGHT, Wouter; WECKHUYSEN, Sarah et al.Acta neurologica belgica. 2008, Vol 108, Num 2, pp 64-66, issn 0300-9009, 3 p.Article

The use of the pedicled supraclavicular flap in noma reconstructive surgeryHARTMAN, Ed. H. M; VAN DAMME, Philip A; SAUTER, Hartwig et al.Journal of plastic, reconstructive & aesthetic surgery. 2006, Vol 59, Num 4, pp 337-342, issn 1748-6815, 6 p.Article

Vascular endothelial growth factor in amyotrophic lateral sclerosis and other neurodegenerative diseasesBOGAERT, Elke; VAN DAMME, Philip; VAN DEN BOSCH, Ludo et al.Muscle & nerve. 2006, Vol 34, Num 4, pp 391-405, issn 0148-639X, 15 p.Article

GluR2 deficiency accelerates motor neuron degeneration in a mouse model of amyotrophic lateral sclerosisVAN DAMME, Philip; BRAEKEN, Dries; CALLEWAERT, Geert et al.Journal of neuropathology and experimental neurology. 2005, Vol 64, Num 7, pp 605-612, issn 0022-3069, 8 p.Article

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisHERDEWYN, Sarah; HUI ZHAO; ROBBERECHT, Wim et al.Human molecular genetics (Print). 2012, Vol 21, Num 11, pp 2412-2419, issn 0964-6906, 8 p.Article

Upregulation of HSP27 in a transgenic model of ALSVLEMINCKX, Vicky; VAN DAMME, Philip; GOFFIN, Karolien et al.Journal of neuropathology and experimental neurology. 2002, Vol 61, Num 11, pp 968-974, issn 0022-3069, 7 p.Article

Serum Biomarker for Progranulin-Associated Frontotemporal Lobar DegenerationSLEEGERS, Kristel; BROUWERS, Nathalie; DE DEYN, Peter P et al.Annals of neurology. 2009, Vol 65, Num 5, pp 603-609, issn 0364-5134, 7 p.Article

Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosisPHILIPS, Thomas; BENTO-ABREU, Andre; RICHARDSON, William D et al.Brain. 2013, Vol 136, pp 471-482, issn 0006-8950, 12 p., 2Article

NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosisBLAUW, Hylke M; RHEENEN, Wouter Van; CUPPEN, Edwin et al.Human molecular genetics (Print). 2012, Vol 21, Num 11, pp 2497-2502, issn 0964-6906, 6 p.Article

Long-lasting changes in GABA responsiveness in cultured neuronsCHABWINE, Joelle N; VAN DAMME, Philip; EGGERMONT, Jan et al.Neuroscience letters. 2004, Vol 365, Num 1, pp 69-72, issn 0304-3940, 4 p.Article

Pathogenic cysteine mutations affect progranulin function and production of mature granulinsJUN WANG; VAN DAMME, Philip; CRUCHAGA, Carlos et al.Journal of neurochemistry. 2010, Vol 112, Num 5, pp 1305-1315, issn 0022-3042, 11 p.Article

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaZIMON, Magdalena; BAETS, Jonathan; AUER-GRUMBACH, Michaela et al.Nature genetics. 2012, Vol 44, Num 10, pp 1080-1083, issn 1061-4036, 4 p.Article

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisBOGAERT, Elke; GORIS, An; DE JONGHE, Peter et al.Neurobiology of aging. 2012, Vol 33, Num 2, pp 418-420, issn 0197-4580, 3 p.Article

Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral SclerosisVAN ES, Michael A; SCHELHAAS, Helenius J; FUMOTO, Katsumi et al.Annals of neurology. 2011, Vol 70, Num 6, pp 964-973, issn 0364-5134, 10 p.Article

Microglial Upregulation of Progranulin as a Marker of Motor Neuron DegenerationPHILIPS, Thomas; DE MUYNCK, Louis; SCIOT, Raf et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 12, pp 1191-1200, issn 0022-3069, 10 p.Article

Etanercept in the treatment of patients with primary Sjögren's syndrome: A pilot studyZANDBELT, Michiel M; DE WILDE, Peter C. M; VAN DAMME, Philip A et al.Journal of rheumatology. 2004, Vol 31, Num 1, pp 96-101, issn 0315-162X, 6 p.Article

Induction of haemarthrosis in the TMJ of rats : Validation by MR imaging (MRI) and histologyALONS, Kai; NAPHAUSEN, Manon T. P; VON DEN HOFF, Johannes W et al.Journal of cranio-maxillo-facial surgery. 2009, Vol 37, Num 3, pp 140-144, issn 1010-5182, 5 p.Article

  • Page / 1