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Channa Maayan

Showing results (1-10 of 33) with videos related to

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Paediatric Respiratory Reviews|June 27, 2006
Respiratory aspects of Riley-Day Syndrome: familial dysautonomiaHanna Channa Maayan
The New England Journal of Medicine|September 14, 2018
Dry EyeChanna Maayan, Samuel N Heyman
Harefuah|September 21, 2012
["But I have done the genetic tests...". The obligation to identify genetic carriers and prenatal genetic tests for new mutations]Channa Maayan, Naama Holzer, Natan Rosenfeld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 12, 2012
Lack of migraine in headaches of familial dysautonomia patientsBoris Shihman, Israel Steiner, Ivelin Yovchev, et al.
Annual Review of Pharmacology and Toxicology|July 9, 2025
Human Mutations in the TRPV1 Channel: Implications for Noxious Cold SensationBen Katz, Rita Gutorov, Channa Maayan, et al.
The Israel Medical Association Journal : IMAJ|November 17, 2009
Chest computed tomography findings in familial dysautonomia patients: a model for aspirationNurith Hiller, Natalia Simanovsky, Chaya Bahagon, et al.
Human Molecular Genetics|June 27, 2007
IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelinationDavid Cheishvili, Channa Maayan, Yoav Smith, et al.
The Journal of Pediatrics|October 16, 2002
Survival in familial dysautonomia: Impact of early interventionFelicia B Axelrod, Judith D Goldberg, Xiang Y Ye, et al.
Clinical Pediatrics|December 26, 2014
Laughter is not always funny: breath-holding spells in familial dysautonomiaChanna Maayan, Eliot Katz, Michal Begin, et al.
Plos One|January 7, 2011
Phosphatidylserine increases IKBKAP levels in familial dysautonomia cellsHadas Keren, Maya Donyo, David Zeevi, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Paediatric Respiratory Reviews|June 27, 2006
Respiratory aspects of Riley-Day Syndrome: familial dysautonomiaHanna Channa Maayan
The New England Journal of Medicine|September 14, 2018
Dry EyeChanna Maayan, Samuel N Heyman
Harefuah|September 21, 2012
["But I have done the genetic tests...". The obligation to identify genetic carriers and prenatal genetic tests for new mutations]Channa Maayan, Naama Holzer, Natan Rosenfeld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 12, 2012
Lack of migraine in headaches of familial dysautonomia patientsBoris Shihman, Israel Steiner, Ivelin Yovchev, et al.
Annual Review of Pharmacology and Toxicology|July 9, 2025
Human Mutations in the TRPV1 Channel: Implications for Noxious Cold SensationBen Katz, Rita Gutorov, Channa Maayan, et al.
The Israel Medical Association Journal : IMAJ|November 17, 2009
Chest computed tomography findings in familial dysautonomia patients: a model for aspirationNurith Hiller, Natalia Simanovsky, Chaya Bahagon, et al.
Human Molecular Genetics|June 27, 2007
IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelinationDavid Cheishvili, Channa Maayan, Yoav Smith, et al.
The Journal of Pediatrics|October 16, 2002
Survival in familial dysautonomia: Impact of early interventionFelicia B Axelrod, Judith D Goldberg, Xiang Y Ye, et al.
Clinical Pediatrics|December 26, 2014
Laughter is not always funny: breath-holding spells in familial dysautonomiaChanna Maayan, Eliot Katz, Michal Begin, et al.
Plos One|January 7, 2011
Phosphatidylserine increases IKBKAP levels in familial dysautonomia cellsHadas Keren, Maya Donyo, David Zeevi, et al.
Pageof 4