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Neda Zadeh

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Prenatal Diagnosis|February 3, 2011
Nuchal translucency measurement in fetuses with spinal muscular atrophyNeda Zadeh, Louanne Hudgins, Mary E Norton
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2011
Diagnosis and management of familial Mediterranean fever: integrating medical genetics in a dedicated interdisciplinary clinicNeda Zadeh, Terri Getzug, Wayne W Grody
American Journal of Obstetrics and Gynecology|June 18, 2002
The effects of cardiovascular dynamics monitoring in the outpatient management of pregnancy hypertensionTeiichiro Fukushima, Maria Berumen, Noemi Vargas, et al.
Applied Microbiology and Biotechnology|August 15, 2025
Advanced monolayer and layer-by-layer nanocapsule systems for sustained release of carvacrol and trans-cinnamaldehyde against multidrug-resistant Salmonella in poultrySamah Mechmechani, Kosar Zadeh, Neda Zadeh, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|July 11, 2025
Cardiac pathology in a patient with a novel pathogenic variant c.703del (p.Ile235SerfsTer4) of the TAFAZZIN geneMarisa Prasanpanich, Majid Husain, Nancy J Halnon, et al.
American Journal of Medical Genetics. Part A|November 18, 2014
Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defectsMarie-Luise Brennan, Margaret P Adam, Laurie H Seaver, et al.
American Journal of Medical Genetics. Part A|September 21, 2011
Ectopia lentis as the presenting and primary feature in Marfan syndromeNeda Zadeh, Jonathan A Bernstein, Anna Kaisa Niemi, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
KCNK9 imprinting syndrome-further delineation of a possible treatable disorderJohn M Graham, Neda Zadeh, Melissa Kelley, et al.
American Journal of Medical Genetics. Part A|November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics|March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delayValerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|February 3, 2011
Nuchal translucency measurement in fetuses with spinal muscular atrophyNeda Zadeh, Louanne Hudgins, Mary E Norton
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2011
Diagnosis and management of familial Mediterranean fever: integrating medical genetics in a dedicated interdisciplinary clinicNeda Zadeh, Terri Getzug, Wayne W Grody
American Journal of Obstetrics and Gynecology|June 18, 2002
The effects of cardiovascular dynamics monitoring in the outpatient management of pregnancy hypertensionTeiichiro Fukushima, Maria Berumen, Noemi Vargas, et al.
Applied Microbiology and Biotechnology|August 15, 2025
Advanced monolayer and layer-by-layer nanocapsule systems for sustained release of carvacrol and trans-cinnamaldehyde against multidrug-resistant Salmonella in poultrySamah Mechmechani, Kosar Zadeh, Neda Zadeh, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|July 11, 2025
Cardiac pathology in a patient with a novel pathogenic variant c.703del (p.Ile235SerfsTer4) of the TAFAZZIN geneMarisa Prasanpanich, Majid Husain, Nancy J Halnon, et al.
American Journal of Medical Genetics. Part A|November 18, 2014
Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defectsMarie-Luise Brennan, Margaret P Adam, Laurie H Seaver, et al.
American Journal of Medical Genetics. Part A|September 21, 2011
Ectopia lentis as the presenting and primary feature in Marfan syndromeNeda Zadeh, Jonathan A Bernstein, Anna Kaisa Niemi, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
KCNK9 imprinting syndrome-further delineation of a possible treatable disorderJohn M Graham, Neda Zadeh, Melissa Kelley, et al.
American Journal of Medical Genetics. Part A|November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics|March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delayValerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Pageof 2