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Rida Jaber

5PUBLICATIONS

12CO-AUTHORS

Anthropological geneticsPaediatrics not elsewhere classifiedInfant and child healthFoetal development and medicineMedical infection agents (incl. prions)

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Publications (5)

Sort by Publication Date:

|Jan 21, 2026

Allgrove syndrome with early neurodegeneration in a child: A case report from Syria.

Hadi Salame, Rida Jaber, Hussein Taher

|Jul 27, 2025

Extremely rare case report of CEBALID syndrome presenting as congenital arthrogryposis.

Fatima A Dirani, Ghina Kahil, Rida Jaber

|Nov 05, 2024

Pyridoxine-dependent epilepsy caused by an ALDH7A1 mutation in an infant girl: the first case report in Syria.

Rida Jaber, Hadi Salame, Mostafa Zeindeen

|Dec 07, 2023

Solitary atrial Rhabdomyoma in an infant with tuberous sclerosis: a case report and review of the literature.

Ali Jawad, Zein Alabdin Hannouneh, Hadi Salame

|Sep 25, 2023

Pulmonary pseudoaneurysm in the setting of concurrent COVID-19 and pulmonary mucormycosis: A rare case report.

Hussein Hamdar, Ali Alakbar Nahle, Rida Jaber

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Frequent Collaborators

4 joint publications

Hadi Salame

2 joint publications

Ali Jawad

1 joint publications

Hussein Hamdar

1 joint publications

Ali Alakbar Nahle

1 joint publications

Amjad Sikaria

1 joint publications

Zein Alabdin Hannouneh

1 joint publications

Mostafa Zeindeen

1 joint publications

Hassan Fawaz

1 joint publications

Fatima A Dirani

1 joint publications

Hussein Taher

Frequent Collaborators

4 joint publications

Hadi Salame

2 joint publications

Ali Jawad

1 joint publications

Hussein Hamdar

1 joint publications

Ali Alakbar Nahle

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