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Ariana Kariminejad

Showing results (1-10 of 123) with videos related to

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CEN Case Reports|May 17, 2017
Juvenile nephronophthisis and dysthyroidism: a rare associationFateme Shamekhi Amiri, Ariana Kariminejad
American Journal of Medical Genetics. Part A|September 20, 2012
Aphonia, microstomia, deafness, retinal dystrophy, duplicated halluces and intellectual disabilityAriana Kariminejad, Raoul C M Hennekam
Interactive Cardiovascular and Thoracic Surgery|February 2, 2010
Absent pulmonary valve, intact interventricular septum, rudimentary aortic non-coronary cusp and ascending aortic aneurysm in a single patientAshkan Karimi, Farah Peiravian, Ahmad Ali Amirghofran, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Amelia, cleft lip, and holoprosencephaly: a distinct entityAriana Kariminejad, Payman Goodarzi, Alaleh Asghari-Roodsari, et al.
Fetal and Pediatric Pathology|March 22, 2012
An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndromeAriana Kariminejad, Siavash Ghaderi-Sohi, Mohammad Hassan Kariminejad, et al.
Clinical Dysmorphology|June 11, 2008
Skull defects, alopecia and distinctive facies: a new syndrome?Ariana Kariminejad, Bita Bozorgmehr, Mahmoud R Ashrafi, et al.
Saudi Medical Journal|January 14, 2009
Restrictive dermopathy. Molecular diagnosis of restrictive dermopathy in a stillborn fetus from a consanguineous Iranian familyAriana Kariminejad, Peyman Goodarzi, Le Thi Thanh Huong, et al.
International Journal of Dermatology|July 30, 2015
Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from IranMohammadreza Barzegar, Zahra Asadi-Kani, Nikoo Mozafari, et al.
Iranian Journal of Pediatrics|October 12, 2012
Ehlers-Danlos Syndrome Type VI in a 17-Year-Old Iranian Boy with Severe Muscular Weakness - A Diagnostic Challenge?Ariana Kariminejad, Bita Bozorgmehr, Alireza Khatami, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Clinical variability in acro-cardio-facial-syndromeAriana Kariminejad, Bita Bozorgmehr, Mohammad Ali Sedighi Gilani, et al.
Pageof 13

Showing results (1-10 of 123) with videos related to

Sort By:
Pageof 13
CEN Case Reports|May 17, 2017
Juvenile nephronophthisis and dysthyroidism: a rare associationFateme Shamekhi Amiri, Ariana Kariminejad
American Journal of Medical Genetics. Part A|September 20, 2012
Aphonia, microstomia, deafness, retinal dystrophy, duplicated halluces and intellectual disabilityAriana Kariminejad, Raoul C M Hennekam
Interactive Cardiovascular and Thoracic Surgery|February 2, 2010
Absent pulmonary valve, intact interventricular septum, rudimentary aortic non-coronary cusp and ascending aortic aneurysm in a single patientAshkan Karimi, Farah Peiravian, Ahmad Ali Amirghofran, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Amelia, cleft lip, and holoprosencephaly: a distinct entityAriana Kariminejad, Payman Goodarzi, Alaleh Asghari-Roodsari, et al.
Fetal and Pediatric Pathology|March 22, 2012
An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndromeAriana Kariminejad, Siavash Ghaderi-Sohi, Mohammad Hassan Kariminejad, et al.
Clinical Dysmorphology|June 11, 2008
Skull defects, alopecia and distinctive facies: a new syndrome?Ariana Kariminejad, Bita Bozorgmehr, Mahmoud R Ashrafi, et al.
Saudi Medical Journal|January 14, 2009
Restrictive dermopathy. Molecular diagnosis of restrictive dermopathy in a stillborn fetus from a consanguineous Iranian familyAriana Kariminejad, Peyman Goodarzi, Le Thi Thanh Huong, et al.
International Journal of Dermatology|July 30, 2015
Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from IranMohammadreza Barzegar, Zahra Asadi-Kani, Nikoo Mozafari, et al.
Iranian Journal of Pediatrics|October 12, 2012
Ehlers-Danlos Syndrome Type VI in a 17-Year-Old Iranian Boy with Severe Muscular Weakness - A Diagnostic Challenge?Ariana Kariminejad, Bita Bozorgmehr, Alireza Khatami, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Clinical variability in acro-cardio-facial-syndromeAriana Kariminejad, Bita Bozorgmehr, Mohammad Ali Sedighi Gilani, et al.
Pageof 13