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Pediatric Dermatology
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July 19, 2022
Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders
Lihi Atzmony, Nelson Ugwu, Claire Hamilton, et al.
Journal of Medical Case Reports
|
January 25, 2025
An atypical presentation of autoimmune hepatitis with delayed menarche in a Nigerian adolescent: a case report
Promise Udoka Asogwa, Bruno Basil, Winifred Njideka Adiri, et al.
American Journal of Medical Genetics. Part A
|
August 16, 2022
Segmental basaloid follicular hamartomas derive from a post-zygotic SMO p.L412F pathogenic variant and express hair follicle development-related proteins in a pattern that distinguish them from basal cell carcinomas
Lihi Atzmony, Nelson Ugwu, Lionel G Bercovitch, et al.
HGG Advances
|
January 20, 2022
Erratum: Cutaneous and hepatic vascular lesions due to a recurrent somatic <i>GJA4</i> mutation reveal a pathway for vascular malformation
Nelson Ugwu, Lihi Atzmony, Katharine T Ellis, et al.
HGG Advances
|
April 29, 2021
Cutaneous and hepatic vascular lesions due to a recurrent somatic <i>GJA4</i> mutation reveal a pathway for vascular malformation
Nelson Ugwu, Lihi Atzmony, Katharine T Ellis, et al.
Genes
|
September 28, 2021
The Genetic Architecture of a Congenital Heart Defect Is Related to Its Fitness Cost
Ehiole Akhirome, Suk D Regmi, Rachel A Magnan, et al.
Molecular and Cellular Endocrinology
|
August 25, 2016
Transgenerational cardiology: One way to a baby's heart is through the mother
Patrick Y Jay, Ehiole Akhirome, Rachel A Magnan, et al.
Human Mutation
|
July 21, 2021
Epistatic interaction of PDE4DIP and DES mutations in familial atrial fibrillation with slow conduction
Maen D Abou Ziki, Neha Bhat, Arpita Neogi, et al.
JAMA Dermatology
|
January 14, 2026
De Novo Germline L858R EGFR Variants and Generalized Acanthosis Nigricans
Xingyuan Jiang, Mark Y Jeng, Zhou Yang, et al.
Nature Genetics
|
July 31, 2019
CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation
Fatemehsadat Esteghamat, James S Broughton, Emily Smith, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Pediatric Dermatology
|
July 19, 2022
Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders
Lihi Atzmony, Nelson Ugwu, Claire Hamilton, et al.
Journal of Medical Case Reports
|
January 25, 2025
An atypical presentation of autoimmune hepatitis with delayed menarche in a Nigerian adolescent: a case report
Promise Udoka Asogwa, Bruno Basil, Winifred Njideka Adiri, et al.
American Journal of Medical Genetics. Part A
|
August 16, 2022
Segmental basaloid follicular hamartomas derive from a post-zygotic SMO p.L412F pathogenic variant and express hair follicle development-related proteins in a pattern that distinguish them from basal cell carcinomas
Lihi Atzmony, Nelson Ugwu, Lionel G Bercovitch, et al.
HGG Advances
|
January 20, 2022
Erratum: Cutaneous and hepatic vascular lesions due to a recurrent somatic <i>GJA4</i> mutation reveal a pathway for vascular malformation
Nelson Ugwu, Lihi Atzmony, Katharine T Ellis, et al.
HGG Advances
|
April 29, 2021
Cutaneous and hepatic vascular lesions due to a recurrent somatic <i>GJA4</i> mutation reveal a pathway for vascular malformation
Nelson Ugwu, Lihi Atzmony, Katharine T Ellis, et al.
Genes
|
September 28, 2021
The Genetic Architecture of a Congenital Heart Defect Is Related to Its Fitness Cost
Ehiole Akhirome, Suk D Regmi, Rachel A Magnan, et al.
Molecular and Cellular Endocrinology
|
August 25, 2016
Transgenerational cardiology: One way to a baby's heart is through the mother
Patrick Y Jay, Ehiole Akhirome, Rachel A Magnan, et al.
Human Mutation
|
July 21, 2021
Epistatic interaction of PDE4DIP and DES mutations in familial atrial fibrillation with slow conduction
Maen D Abou Ziki, Neha Bhat, Arpita Neogi, et al.
JAMA Dermatology
|
January 14, 2026
De Novo Germline L858R EGFR Variants and Generalized Acanthosis Nigricans
Xingyuan Jiang, Mark Y Jeng, Zhou Yang, et al.
Nature Genetics
|
July 31, 2019
CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation
Fatemehsadat Esteghamat, James S Broughton, Emily Smith, et al.
Page
of 4