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Pediatric Pulmonology
|
November 8, 2002
Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalacia
Raphael 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 fever
Ruth 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 syndrome
Ana 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 tracheobronchomalacia
Marwan 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 mutation
Ruth Gershoni-Baruch, Riva Brik, Merav Lidar, et al.
Pediatric Pulmonology
|
May 15, 2003
Pulmonary manifestations and function tests in children genetically diagnosed with FMF
Riva Brik, Ruth Gershoni-Baruch, Marwan Shinawi, et al.
Molecular Syndromology
|
June 22, 2018
DeSanto-Shinawi Syndrome: First Case in South America
Sara Vanegas, Diana Ramirez-Montaño, Estephania Candelo, et al.
Pediatric Radiology
|
July 8, 2010
McCune-Albright syndrome presenting with unilateral macroorchidism and bilateral testicular masses
Geetika 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 variability
Ruth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
International Journal of Dermatology
|
May 22, 2012
ADULT syndrome due to an R243W mutation in TP63
David R Berk, Nicole L Armstrong, Marwan Shinawi, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 170) with videos related to
Sort By:
Page
of 17
Pediatric Pulmonology
|
November 8, 2002
Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalacia
Raphael 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 fever
Ruth 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 syndrome
Ana 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 tracheobronchomalacia
Marwan 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 mutation
Ruth Gershoni-Baruch, Riva Brik, Merav Lidar, et al.
Pediatric Pulmonology
|
May 15, 2003
Pulmonary manifestations and function tests in children genetically diagnosed with FMF
Riva Brik, Ruth Gershoni-Baruch, Marwan Shinawi, et al.
Molecular Syndromology
|
June 22, 2018
DeSanto-Shinawi Syndrome: First Case in South America
Sara Vanegas, Diana Ramirez-Montaño, Estephania Candelo, et al.
Pediatric Radiology
|
July 8, 2010
McCune-Albright syndrome presenting with unilateral macroorchidism and bilateral testicular masses
Geetika 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 variability
Ruth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
International Journal of Dermatology
|
May 22, 2012
ADULT syndrome due to an R243W mutation in TP63
David R Berk, Nicole L Armstrong, Marwan Shinawi, et al.
Page
of 17