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S Quijano-Roy

Showing results (1-10 of 25) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Clinical features of spinal muscular atrophy (SMA) type 3 (Kugelberg-Welander disease)E Salort-Campana, S Quijano-Roy
Anales Espanoles De Pediatria|December 22, 1998
[Smith-Magenis syndrome: a case report]S Quijano Roy, A Delicado Navarro, I López Pajares, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 5, 2017
[The place of neuropathy in the early diagnosis of Cockayne syndrome: Report on two siblings]N Blin-Rochemaure, N Allani-Essid, R Carlier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 13, 2006
[Campylobacter jejuni and cytomegalovirus (CMV) infections in patients with the Guillain-Barre syndrome]D Orlikowski, S Quijano-Roy, V Sivadon-Tardy, et al.
Anales Espanoles De Pediatria|February 10, 2000
[Type I neurofibromatosis associated with internal carotid artery hypoplasia]U Barcik, S Quijano-Roy, M A Caballero-Martín, et al.
Diagnostic and Interventional Imaging|May 1, 2012
Axonotmesis of the sciatic nerveM Ohana, S Quijano-Roy, F Colas, et al.
Anales Espanoles De Pediatria|June 1, 1997
[Smith-Lemli-Opitz syndrome: abnormal cholesterol biosynthesis]M de la Torre Verdú, M Vázquez López, L Carrasco Marina, et al.
Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, et al.
Revista De Neurologia|June 16, 2006
[Cerebellar ataxia of Norman-Jaeken. Presentation of seven Spanish patients]I Pascual-Castroviejo, S I Pascual-Pascual, S Quijano-Roy, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Clinical features of spinal muscular atrophy (SMA) type 3 (Kugelberg-Welander disease)E Salort-Campana, S Quijano-Roy
Anales Espanoles De Pediatria|December 22, 1998
[Smith-Magenis syndrome: a case report]S Quijano Roy, A Delicado Navarro, I López Pajares, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 5, 2017
[The place of neuropathy in the early diagnosis of Cockayne syndrome: Report on two siblings]N Blin-Rochemaure, N Allani-Essid, R Carlier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 13, 2006
[Campylobacter jejuni and cytomegalovirus (CMV) infections in patients with the Guillain-Barre syndrome]D Orlikowski, S Quijano-Roy, V Sivadon-Tardy, et al.
Anales Espanoles De Pediatria|February 10, 2000
[Type I neurofibromatosis associated with internal carotid artery hypoplasia]U Barcik, S Quijano-Roy, M A Caballero-Martín, et al.
Diagnostic and Interventional Imaging|May 1, 2012
Axonotmesis of the sciatic nerveM Ohana, S Quijano-Roy, F Colas, et al.
Anales Espanoles De Pediatria|June 1, 1997
[Smith-Lemli-Opitz syndrome: abnormal cholesterol biosynthesis]M de la Torre Verdú, M Vázquez López, L Carrasco Marina, et al.
Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, et al.
Revista De Neurologia|June 16, 2006
[Cerebellar ataxia of Norman-Jaeken. Presentation of seven Spanish patients]I Pascual-Castroviejo, S I Pascual-Pascual, S Quijano-Roy, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Pageof 3