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Hagit Baris

Showing results (1-10 of 96) with videos related to

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Human Genetics|April 27, 2023
Special issue: the genetics of early onset inflammatory bowel disease (IBD) and diarrheal disordersAlina Kurolap, Hagit Baris Feldman
British Journal of Haematology|March 25, 2010
Diagnosis of severe type 1 Gaucher's disease before irreversible damage occurs : is HDL cholesterol the answer?Ian J Cohen, Isaac Yaniv, Hagit Baris
The New England Journal of Medicine|April 24, 2024
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and Fibrosis. ReplyAlina Kurolap, Chofit Chai Gadot, Hagit Baris Feldman
American Journal of Medical Genetics. Part A|February 16, 2005
Hypothelia, syndactyly, and ear malformation--a variant of the scalp-ear-nipple syndrome?: Case report and review of the literatureHagit Baris, Wen-Hann Tan, Virginia E Kimonis
Pediatric Endocrinology Reviews : PER|January 2, 2014
Treatment for LSDs: no longer just enzyme replacement therapy for Gaucher disease. ForewordIan J Cohen, Hagit Baris, Pramod Kumar Mistry
Journal of Child Neurology|January 19, 2006
Krabbe disease: severe neonatal presentation with a family history of multiple sclerosisInderneel Sahai, Hagit Baris, Virginia Kimonis, et al.
Rambam Maimonides Medical Journal|July 16, 2021
Non-immune Hemolysis in Gaucher Disease and Review of the LiteratureEliyakim Hershkop, Idan Bergman, Alina Kurolap, et al.
Pediatric Endocrinology Reviews : PER|August 6, 2016
Overcoming the Next Barriers to Successful TherapyIan J Cohen, Hagit Baris, Pramod Kumar Mistry, et al.
American Journal of Medical Genetics. Part A|February 1, 2024
PUF60 loss-of-function with normal cognition should be considered in the differential diagnosis of Klippel-Feil syndromeMichal Yacobi Bach, Sivan Reytan Miron, Alina Kurolap, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Cockayne syndrome: the developing phenotypeWen-Hann Tan, Hagit Baris, Caroline D Robson, et al.
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
Human Genetics|April 27, 2023
Special issue: the genetics of early onset inflammatory bowel disease (IBD) and diarrheal disordersAlina Kurolap, Hagit Baris Feldman
British Journal of Haematology|March 25, 2010
Diagnosis of severe type 1 Gaucher's disease before irreversible damage occurs : is HDL cholesterol the answer?Ian J Cohen, Isaac Yaniv, Hagit Baris
The New England Journal of Medicine|April 24, 2024
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and Fibrosis. ReplyAlina Kurolap, Chofit Chai Gadot, Hagit Baris Feldman
American Journal of Medical Genetics. Part A|February 16, 2005
Hypothelia, syndactyly, and ear malformation--a variant of the scalp-ear-nipple syndrome?: Case report and review of the literatureHagit Baris, Wen-Hann Tan, Virginia E Kimonis
Pediatric Endocrinology Reviews : PER|January 2, 2014
Treatment for LSDs: no longer just enzyme replacement therapy for Gaucher disease. ForewordIan J Cohen, Hagit Baris, Pramod Kumar Mistry
Journal of Child Neurology|January 19, 2006
Krabbe disease: severe neonatal presentation with a family history of multiple sclerosisInderneel Sahai, Hagit Baris, Virginia Kimonis, et al.
Rambam Maimonides Medical Journal|July 16, 2021
Non-immune Hemolysis in Gaucher Disease and Review of the LiteratureEliyakim Hershkop, Idan Bergman, Alina Kurolap, et al.
Pediatric Endocrinology Reviews : PER|August 6, 2016
Overcoming the Next Barriers to Successful TherapyIan J Cohen, Hagit Baris, Pramod Kumar Mistry, et al.
American Journal of Medical Genetics. Part A|February 1, 2024
PUF60 loss-of-function with normal cognition should be considered in the differential diagnosis of Klippel-Feil syndromeMichal Yacobi Bach, Sivan Reytan Miron, Alina Kurolap, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Cockayne syndrome: the developing phenotypeWen-Hann Tan, Hagit Baris, Caroline D Robson, et al.
Pageof 10