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Neuropediatrics
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May 7, 2010
Normal cognitive functions in joubert syndrome
A Poretti, F Dietrich Alber, F Brancati, et al.
Stem Cell Research
|
December 15, 2022
Generation of an iPSC line from skin fibroblasts of a patient with Joubert syndrome carrying the homozygous loss of function variant c.787dupC in the AHI1 gene
V Serpieri, A Orsi, C Mazzotta, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 24, 1999
Italian family with cranial cervical dystonia: clinical and genetic study
E Cassetta, N Del Grosso, A R Bentivoglio, et al.
Neurology
|
June 16, 2005
The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease
A Albanese, E M Valente, L M Romito, et al.
Eye (London, England)
|
May 23, 2009
Ophthalmological findings in Joubert syndrome
V Sturm, H Leiba, M N Menke, et al.
Stem Cell Research
|
February 14, 2024
Generation of iPSC lines derived from skin fibroblasts of two healthy controls using non-transmissible form of Sendai Virus
A Orsi, V Serpieri, C Mazzotta, et al.
Journal of Medical Genetics
|
November 25, 2003
Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14
F Brancati, E M Valente, G Tadini, et al.
Acta Neurologica Scandinavica
|
November 1, 1996
Surgical prognosis in carpal tunnel syndrome: usefulness of a preoperative neurophysiological assessment
L Padua, M LoMonaco, L Aulisa, et al.
European Journal of Neurology
|
January 30, 2014
Recurrent and fatal akinetic crisis in genetic-mitochondrial parkinsonisms
L Bonanni, M Onofrj, E M Valente, et al.
Journal of Neurology
|
April 6, 2000
Phenotype variability of dystonia in monozygotic twins
A Albanese, A R Bentivoglio, N Del Grosso, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 61) with videos related to
Sort By:
Page
of 7
Neuropediatrics
|
May 7, 2010
Normal cognitive functions in joubert syndrome
A Poretti, F Dietrich Alber, F Brancati, et al.
Stem Cell Research
|
December 15, 2022
Generation of an iPSC line from skin fibroblasts of a patient with Joubert syndrome carrying the homozygous loss of function variant c.787dupC in the AHI1 gene
V Serpieri, A Orsi, C Mazzotta, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 24, 1999
Italian family with cranial cervical dystonia: clinical and genetic study
E Cassetta, N Del Grosso, A R Bentivoglio, et al.
Neurology
|
June 16, 2005
The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease
A Albanese, E M Valente, L M Romito, et al.
Eye (London, England)
|
May 23, 2009
Ophthalmological findings in Joubert syndrome
V Sturm, H Leiba, M N Menke, et al.
Stem Cell Research
|
February 14, 2024
Generation of iPSC lines derived from skin fibroblasts of two healthy controls using non-transmissible form of Sendai Virus
A Orsi, V Serpieri, C Mazzotta, et al.
Journal of Medical Genetics
|
November 25, 2003
Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14
F Brancati, E M Valente, G Tadini, et al.
Acta Neurologica Scandinavica
|
November 1, 1996
Surgical prognosis in carpal tunnel syndrome: usefulness of a preoperative neurophysiological assessment
L Padua, M LoMonaco, L Aulisa, et al.
European Journal of Neurology
|
January 30, 2014
Recurrent and fatal akinetic crisis in genetic-mitochondrial parkinsonisms
L Bonanni, M Onofrj, E M Valente, et al.
Journal of Neurology
|
April 6, 2000
Phenotype variability of dystonia in monozygotic twins
A Albanese, A R Bentivoglio, N Del Grosso, et al.
Page
of 7