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Journal of Pediatric Gastroenterology and Nutrition
|
November 26, 2009
Early-onset Crohn disease is associated with male sex and a polymorphism in the IL-6 promoter
Keren Sagiv-Friedgut, Amir Karban, Batya Weiss, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 14, 2016
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
Daniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
The American Journal of Gastroenterology
|
June 30, 2005
TNF promoter polymorphisms and modulation of growth retardation and disease severity in pediatric Crohn's disease
Arie Levine, Raanan Shamir, Eytan Wine, et al.
Inflammatory Bowel Diseases
|
January 1, 2005
NOD2/CARD15 mutations and presence of granulomas in pediatric and adult Crohn's disease
Ron Shaoul, Amir Karban, Batia Weiss, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions
Esther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Inflammatory Bowel Diseases
|
September 1, 2007
Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility
Arie Levine, Subra Kugathasan, Vito Annese, et al.
Neurogenetics
|
February 15, 2014
Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene
Lubov Blumkin, Ayelet Halevy, Dominique Ben-Ami-Raichman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 13, 2014
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings
Ayelet Zerem, Dorit Lev, Lubov Blumkin, et al.
Journal of Medical Genetics
|
March 1, 2014
VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)
Miora Feinstein, Hagit Flusser, Tally Lerman-Sagie, et al.
American Journal of Human Genetics
|
October 6, 2010
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy
Orly Agamy, Bruria Ben Zeev, Dorit Lev, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
Journal of Pediatric Gastroenterology and Nutrition
|
November 26, 2009
Early-onset Crohn disease is associated with male sex and a polymorphism in the IL-6 promoter
Keren Sagiv-Friedgut, Amir Karban, Batya Weiss, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 14, 2016
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
Daniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
The American Journal of Gastroenterology
|
June 30, 2005
TNF promoter polymorphisms and modulation of growth retardation and disease severity in pediatric Crohn's disease
Arie Levine, Raanan Shamir, Eytan Wine, et al.
Inflammatory Bowel Diseases
|
January 1, 2005
NOD2/CARD15 mutations and presence of granulomas in pediatric and adult Crohn's disease
Ron Shaoul, Amir Karban, Batia Weiss, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions
Esther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Inflammatory Bowel Diseases
|
September 1, 2007
Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility
Arie Levine, Subra Kugathasan, Vito Annese, et al.
Neurogenetics
|
February 15, 2014
Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene
Lubov Blumkin, Ayelet Halevy, Dominique Ben-Ami-Raichman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 13, 2014
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings
Ayelet Zerem, Dorit Lev, Lubov Blumkin, et al.
Journal of Medical Genetics
|
March 1, 2014
VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)
Miora Feinstein, Hagit Flusser, Tally Lerman-Sagie, et al.
American Journal of Human Genetics
|
October 6, 2010
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy
Orly Agamy, Bruria Ben Zeev, Dorit Lev, et al.
Page
of 7