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Showing results (41-50 of 47) with videos related to

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Neurology|October 12, 2005
Postinfectious inflammatory disorders: subgroups based on prospective follow-upE Marchioni, S Ravaglia, G Piccolo, et al.
Neurology|May 10, 2000
Migraine with aura and white matter abnormalities: Notch3 mutationM Ceroni, T E Poloni, S Tonietti, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 25, 2019
An atypical presentation of diffuse midline pontine glioma in a middle age patient: Case reportS Floro, D Belvedere, C Rosci, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Neurology|October 12, 2005
Postinfectious inflammatory disorders: subgroups based on prospective follow-upE Marchioni, S Ravaglia, G Piccolo, et al.
Neurology|May 10, 2000
Migraine with aura and white matter abnormalities: Notch3 mutationM Ceroni, T E Poloni, S Tonietti, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 25, 2019
An atypical presentation of diffuse midline pontine glioma in a middle age patient: Case reportS Floro, D Belvedere, C Rosci, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 5