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Human Molecular Genetics
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July 13, 2013
Curcumin facilitates a transitory cellular stress response in Trembler-J mice
Yuji Okamoto, Davut Pehlivan, Wojciech Wiszniewski, et al.
Pediatric Neurology
|
June 18, 2022
Assessing the Burden on Caregivers of MECP2 Duplication Syndrome
Muharrem Ak, Zekeriya Akturk, Kristina Bowyer, et al.
Pediatric Neurology
|
April 12, 2024
A Comprehensive Examination of Clinical Characteristics and Determinants of Long-Term Outcomes in Pediatric Cerebral Sinus Venous Thrombosis
Cemal Karakas, Isabella Herman, Stephen F Kralik, et al.
Pediatric Neurology
|
April 9, 2017
Primary Amebic Meningoencephalitis in Children: A Report of Two Fatal Cases and Review of the Literature
Robert C Stowe, Davut Pehlivan, Katie E Friederich, et al.
The Tokai Journal of Experimental and Clinical Medicine
|
July 20, 2011
Esophagus cancer and IgA deficiency in a patient with Dubowitz syndrome: a case report
Ibrahim Halil Turkbeyler, Yavuz Pehlivan, Gazi Comez, et al.
BMC Medical Genomics
|
April 15, 2024
Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt-Yozgatli, Davut Pehlivan, Richard A Gibbs, et al.
Molecular Genetics & Genomic Medicine
|
June 15, 2022
Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent-oriented outcome measures
Muharrem Ak, Bernhard Suter, Zekeriya Akturk, et al.
BMC Medical Genomics
|
August 7, 2024
Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt-Yozgatli, Davut Pehlivan, Richard A Gibbs, et al.
The Journal of Dermatology
|
October 9, 2012
A Turkish trichothiodystrophy patient with homozygous XPD mutation and genotype-phenotype relationship
Davut Pehlivan, Kivanc Cefle, Anja Raams, et al.
Journal of Child Neurology
|
September 26, 2024
Cerebral Sinus Venous Thrombosis in Pediatric Acute Lymphoblastic Leukemia: Incidence, Clinical Characteristics, and Long-term Neurologic Outcomes
Lindsay Johnson-Bishop, Cemal Karakas, Stephen F Kralik, et al.
Page
of 15
Search research articles
Search
Showing results (11-20 of 146) with videos related to
Sort By:
Page
of 15
Human Molecular Genetics
|
July 13, 2013
Curcumin facilitates a transitory cellular stress response in Trembler-J mice
Yuji Okamoto, Davut Pehlivan, Wojciech Wiszniewski, et al.
Pediatric Neurology
|
June 18, 2022
Assessing the Burden on Caregivers of MECP2 Duplication Syndrome
Muharrem Ak, Zekeriya Akturk, Kristina Bowyer, et al.
Pediatric Neurology
|
April 12, 2024
A Comprehensive Examination of Clinical Characteristics and Determinants of Long-Term Outcomes in Pediatric Cerebral Sinus Venous Thrombosis
Cemal Karakas, Isabella Herman, Stephen F Kralik, et al.
Pediatric Neurology
|
April 9, 2017
Primary Amebic Meningoencephalitis in Children: A Report of Two Fatal Cases and Review of the Literature
Robert C Stowe, Davut Pehlivan, Katie E Friederich, et al.
The Tokai Journal of Experimental and Clinical Medicine
|
July 20, 2011
Esophagus cancer and IgA deficiency in a patient with Dubowitz syndrome: a case report
Ibrahim Halil Turkbeyler, Yavuz Pehlivan, Gazi Comez, et al.
BMC Medical Genomics
|
April 15, 2024
Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt-Yozgatli, Davut Pehlivan, Richard A Gibbs, et al.
Molecular Genetics & Genomic Medicine
|
June 15, 2022
Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent-oriented outcome measures
Muharrem Ak, Bernhard Suter, Zekeriya Akturk, et al.
BMC Medical Genomics
|
August 7, 2024
Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt-Yozgatli, Davut Pehlivan, Richard A Gibbs, et al.
The Journal of Dermatology
|
October 9, 2012
A Turkish trichothiodystrophy patient with homozygous XPD mutation and genotype-phenotype relationship
Davut Pehlivan, Kivanc Cefle, Anja Raams, et al.
Journal of Child Neurology
|
September 26, 2024
Cerebral Sinus Venous Thrombosis in Pediatric Acute Lymphoblastic Leukemia: Incidence, Clinical Characteristics, and Long-term Neurologic Outcomes
Lindsay Johnson-Bishop, Cemal Karakas, Stephen F Kralik, et al.
Page
of 15