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Marwan Shinawi

Showing results (21-30 of 170) with videos related to

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Pediatric Pulmonology|November 8, 2002
Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalaciaRaphael Beck, Andrea L Sertie, Riva Brik, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean feverRuth Gershoni-Baruch, Riva Brik, Marwan Shinawi, et al.
Clinical Hypertension|March 1, 2023
Case report: malignant hypertension associated with catecholamine excess in a patient with Leigh syndromeAna Solis, Joshua Shimony, Marwan Shinawi, et al.
Pediatric Pulmonology|January 25, 2005
Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalaciaMarwan Shinawi, Catherine Boileau, Riva Brik, et al.
The Journal of Rheumatology|February 4, 2003
Male sex coupled with articular manifestations cause a 4-fold increase in susceptibility to amyloidosis in patients with familial Mediterranean fever homozygous for the M694V-MEFV mutationRuth Gershoni-Baruch, Riva Brik, Merav Lidar, et al.
Pediatric Pulmonology|May 15, 2003
Pulmonary manifestations and function tests in children genetically diagnosed with FMFRiva Brik, Ruth Gershoni-Baruch, Marwan Shinawi, et al.
Molecular Syndromology|June 22, 2018
DeSanto-Shinawi Syndrome: First Case in South AmericaSara Vanegas, Diana Ramirez-Montaño, Estephania Candelo, et al.
Pediatric Radiology|July 8, 2010
McCune-Albright syndrome presenting with unilateral macroorchidism and bilateral testicular massesGeetika Khanna, Kartikeya Kantawala, Marwan Shinawi, et al.
American Journal of Medical Genetics|April 27, 2002
Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variabilityRuth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
International Journal of Dermatology|May 22, 2012
ADULT syndrome due to an R243W mutation in TP63David R Berk, Nicole L Armstrong, Marwan Shinawi, et al.
Pageof 17

Showing results (21-30 of 170) with videos related to

Sort By:
Pageof 17
Pediatric Pulmonology|November 8, 2002
Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalaciaRaphael Beck, Andrea L Sertie, Riva Brik, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean feverRuth Gershoni-Baruch, Riva Brik, Marwan Shinawi, et al.
Clinical Hypertension|March 1, 2023
Case report: malignant hypertension associated with catecholamine excess in a patient with Leigh syndromeAna Solis, Joshua Shimony, Marwan Shinawi, et al.
Pediatric Pulmonology|January 25, 2005
Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalaciaMarwan Shinawi, Catherine Boileau, Riva Brik, et al.
The Journal of Rheumatology|February 4, 2003
Male sex coupled with articular manifestations cause a 4-fold increase in susceptibility to amyloidosis in patients with familial Mediterranean fever homozygous for the M694V-MEFV mutationRuth Gershoni-Baruch, Riva Brik, Merav Lidar, et al.
Pediatric Pulmonology|May 15, 2003
Pulmonary manifestations and function tests in children genetically diagnosed with FMFRiva Brik, Ruth Gershoni-Baruch, Marwan Shinawi, et al.
Molecular Syndromology|June 22, 2018
DeSanto-Shinawi Syndrome: First Case in South AmericaSara Vanegas, Diana Ramirez-Montaño, Estephania Candelo, et al.
Pediatric Radiology|July 8, 2010
McCune-Albright syndrome presenting with unilateral macroorchidism and bilateral testicular massesGeetika Khanna, Kartikeya Kantawala, Marwan Shinawi, et al.
American Journal of Medical Genetics|April 27, 2002
Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variabilityRuth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
International Journal of Dermatology|May 22, 2012
ADULT syndrome due to an R243W mutation in TP63David R Berk, Nicole L Armstrong, Marwan Shinawi, et al.
Pageof 17