Hüseyin Per

11PUBLICATIONS
106CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)NeonatologyCardiology (incl. cardiovascular diseases)Immunogenetics (incl. genetic immunology)
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Publications (11)

|Sep 01, 2026
From Leukaemia to MOGAD, From Refractive Error to Dural Fistula: Torticollis as the Presenting Sign of Serious Disease in Children.

|Jul 19, 2026
"Severe intellectual disability with cardiac and dermatologic involvement due to homozygous METTL23 frameshift mutation: a case report of two Turkish sisters".

|Jul 09, 2026
Clinical phenotypes and early treatment escalation in pediatric acute drug-induced dystonia: A tertiary emergency department cohort study.

|Jan 16, 2025
The clinical presentation and genetic diagnosis of Tangier disease in the pediatric age group.

Selcan Öztürk, Muhammet Ensar Doğan, Banu Kadıoğlu Yılmaz

|Oct 01, 2024
Corrigendum to "A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort": [Turkish Journal of Medical Sciences 54 (1) 2024 86-98].

İzem Olcay Şahin, Emine Karataş, Mikail Demir

|Aug 09, 2024
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans.

Zehra Busra Azizoglu, Royala Babayeva, Zehra Sule Haskologlu

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Frequent Collaborators

3 joint publications

Ayten Güleç

2 joint publications

Büşra Tan

2 joint publications

Zehra Busra Azizoglu

2 joint publications

Busra Aynekin