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Neurogenetics
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November 3, 2021
Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene
Berardo Rinaldi, Yu-Han Ge, Elena Freri, et al.
Neurogenetics
|
May 13, 2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family
Simone Olgiati, Anna De Rosa, Marialuisa Quadri, et al.
Neurogenetics
|
March 24, 2019
Celia's encephalopathy and c.974dupG in BSCL2 gene: a hidden change in a known variant
Sofía Sánchez-Iglesias, Melissa Crocker, Mar O'Callaghan, et al.
Neurogenetics
|
July 4, 2012
RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas
German Melean, Ana Velasco, Elisabete Hernández-Imaz, et al.
Neurogenetics
|
September 15, 2012
Mammalian sleep genetics
Jessica M Kelly, Matt T Bianchi
Neurogenetics
|
September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesis
Alessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Neurogenetics
|
March 23, 2004
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease
Katrina A B Goddard, Jane M Olson, Haydeh Payami, et al.
Neurogenetics
|
March 19, 2005
Novel mutations and repeated findings of mutations in familial Alzheimer disease
Ulrich Finckh, Christian Kuschel, Maria Anagnostouli, et al.
Neurogenetics
|
April 14, 2005
Diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR
Stefano Regis, Serena Grossi, Susanna Lualdi, et al.
Neurogenetics
|
March 3, 2005
Functional polymorphisms in the human beta4 subunit of nicotinic acetylcholine receptors
Yong Liang, Ramiro Salas, Lisa Marubio, et al.
Page
of 95
Search research articles
Search
Showing results (781-790 of 949) with videos related to
Sort By:
Page
of 95
Neurogenetics
|
November 3, 2021
Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene
Berardo Rinaldi, Yu-Han Ge, Elena Freri, et al.
Neurogenetics
|
May 13, 2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family
Simone Olgiati, Anna De Rosa, Marialuisa Quadri, et al.
Neurogenetics
|
March 24, 2019
Celia's encephalopathy and c.974dupG in BSCL2 gene: a hidden change in a known variant
Sofía Sánchez-Iglesias, Melissa Crocker, Mar O'Callaghan, et al.
Neurogenetics
|
July 4, 2012
RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas
German Melean, Ana Velasco, Elisabete Hernández-Imaz, et al.
Neurogenetics
|
September 15, 2012
Mammalian sleep genetics
Jessica M Kelly, Matt T Bianchi
Neurogenetics
|
September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesis
Alessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Neurogenetics
|
March 23, 2004
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease
Katrina A B Goddard, Jane M Olson, Haydeh Payami, et al.
Neurogenetics
|
March 19, 2005
Novel mutations and repeated findings of mutations in familial Alzheimer disease
Ulrich Finckh, Christian Kuschel, Maria Anagnostouli, et al.
Neurogenetics
|
April 14, 2005
Diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR
Stefano Regis, Serena Grossi, Susanna Lualdi, et al.
Neurogenetics
|
March 3, 2005
Functional polymorphisms in the human beta4 subunit of nicotinic acetylcholine receptors
Yong Liang, Ramiro Salas, Lisa Marubio, et al.
Page
of 95