Hassan Vahidnezhad

Incoming Associate professor

Children's Hospital of Philadelphia

United States

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Articles (19)

Collaborators (9)

Alireza Tavasoli

Pediatric Headache Fellowship

Phoenix Children's Hospital

UNITED STATES

Ahmad Yatim

Rockefeller University

UNITED STATES

Sylvia Hsu

Professor and Chair

Temple University Health System

UNITED STATES

Joanna Jackow

King’s College London

UNITED KINGDOM

Mana Momenilandi

Imagine Institute for Genetic Diseases

Jouni Uitto

UNITED STATES

M. Linares‐Barrios

Qiaoli Li

Thomas Jefferson University

UNITED STATES

Jean-Laurent Casanova

Levy Family Professor

Rockefeller University

UNITED STATES

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Hassan Vahidnezhad

Research Interests

Explore related searches

Contact this professor

Articles (19)

Collaborators (9)

Alireza Tavasoli

Ahmad Yatim

Sylvia Hsu

Joanna Jackow

Mana Momenilandi

Jouni Uitto

M. Linares‐Barrios

Qiaoli Li

Jean-Laurent Casanova

Make your next move.

Hassan Vahidnezhad

Research Interests

Explore related searches

Contact this professor

Articles (19)

A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies

Correlation between melphalan chemotherapy with longitudinal global strain indices of the left ventricle in multiple myeloma patients: A velocity vector imaging (VVI) echocardiography study

DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review

RARS1-related hypomyelinating leukodystrophy-9 (HLD-9) in two distinct Iranian families: Case report and literature review

Whole-Transcriptome Sequencing–Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug‐induced associations

Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry (neurogenetics, (2023), 24, 4, (279-289), 10.1007/s10048-023-00730-y)

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/s13023-023-02780-9)

Purpuric dermatosis and lymphocytic vasculopathy following SARS‐CoV ‐2 vaccination: Report of two patients

Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series

De novo severe pemphigus vulgaris following SARS‐CoV ‐2 vaccination with BBIBP‐CorV

Novel splice mutation in CDSN gene causing type b peeling skin syndrome

Whole‐transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late‐onset segmental Darier disease

Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

Advance trends in targeting homology-directed repair for accurate gene editing: An inclusive review of small molecules and modified CRISPR-Cas9 systems

Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

Collaborators (9)

Alireza Tavasoli

Ahmad Yatim

Sylvia Hsu

Joanna Jackow

Mana Momenilandi

Jouni Uitto

M. Linares‐Barrios

Qiaoli Li

Jean-Laurent Casanova

Make your next move.