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Rachel Straussberg

Showing results (61-70 of 85) with videos related to

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Annals of Neurology|May 6, 2003
Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16Bernard S Chang, Xianhua Piao, Adria Bodell, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Blood|November 15, 2012
CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathyYoram Nevo, Bruria Ben-Zeev, Adi Tabib, et al.
Journal of Medical Genetics|April 16, 2011
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGNGal Maydan, Iris Noyman, Adi Har-Zahav, et al.
Science (New York, N.Y.)|March 27, 2004
G protein-coupled receptor-dependent development of human frontal cortexXianhua Piao, R Sean Hill, Adria Bodell, et al.
Epilepsia|June 4, 2014
Early onset epileptic encephalopathy caused by de novo SCN8A mutationsChihiro Ohba, Mitsuhiro Kato, Satoru Takahashi, et al.
American Journal of Human Genetics|March 30, 2020
Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and SeizuresTiong Yang Tan, Jiří Sedmík, Mark P Fitzgerald, et al.
Human Genetics|March 21, 2015
Homozygous MED25 mutation implicated in eye-intellectual disability syndromeLina Basel-Vanagaite, Pola Smirin-Yosef, Jenna Lee Essakow, et al.
Molecular Psychiatry|April 7, 2020
The murine ortholog of Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3ccMateusz C Ambrozkiewicz, Ekaterina Borisova, Manuela Schwark, et al.
Cell Reports|May 18, 2016
The Adhesion G Protein-Coupled Receptor GPR56/ADGRG1 Is an Inhibitory Receptor on Human NK CellsGin-Wen Chang, Cheng-Chih Hsiao, Yen-Ming Peng, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Annals of Neurology|May 6, 2003
Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16Bernard S Chang, Xianhua Piao, Adria Bodell, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Blood|November 15, 2012
CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathyYoram Nevo, Bruria Ben-Zeev, Adi Tabib, et al.
Journal of Medical Genetics|April 16, 2011
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGNGal Maydan, Iris Noyman, Adi Har-Zahav, et al.
Science (New York, N.Y.)|March 27, 2004
G protein-coupled receptor-dependent development of human frontal cortexXianhua Piao, R Sean Hill, Adria Bodell, et al.
Epilepsia|June 4, 2014
Early onset epileptic encephalopathy caused by de novo SCN8A mutationsChihiro Ohba, Mitsuhiro Kato, Satoru Takahashi, et al.
American Journal of Human Genetics|March 30, 2020
Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and SeizuresTiong Yang Tan, Jiří Sedmík, Mark P Fitzgerald, et al.
Human Genetics|March 21, 2015
Homozygous MED25 mutation implicated in eye-intellectual disability syndromeLina Basel-Vanagaite, Pola Smirin-Yosef, Jenna Lee Essakow, et al.
Molecular Psychiatry|April 7, 2020
The murine ortholog of Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3ccMateusz C Ambrozkiewicz, Ekaterina Borisova, Manuela Schwark, et al.
Cell Reports|May 18, 2016
The Adhesion G Protein-Coupled Receptor GPR56/ADGRG1 Is an Inhibitory Receptor on Human NK CellsGin-Wen Chang, Cheng-Chih Hsiao, Yen-Ming Peng, et al.
Pageof 9