Ghassan Mohamadsalih

6PUBLICATIONS
16CO-AUTHORS
Infant and child healthTe Whāriki - te mātauranga kōhungahunga Māori (Māori early childhood education)AutoimmunityNeonatologyAdolescent health
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Publications (6)

|Nov 23, 2025
Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity.

Samar S Hassan, Salwa A Musa, Elisa De Franco

|Sep 04, 2025
Mauriac Syndrome in Sudanese Children: An Old Syndrome Still Existing in Resource-Limited Countries.

Mariam M Ismail, Olivia A Al-Hassan, Ghassan Mohamadsalih

|Jun 02, 2025
Permanent Congenital Hypothyroidism due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis.

|Apr 30, 2025
Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.

Samar S Hassan, Salwa A Musa, Elisa De Franco

|Oct 15, 2021
Clinical profile, etiology, and diagnostic challenges of primary adrenal insufficiency in Sudanese children: 14-years' experience from a resource limited setting.

Salwa A Musa, Samar S Hassan, Amna I Ahmed

|Jul 14, 2020
Autoimmune hyperthyroidism in children & adolescents in Sudan: a 13 years' experience of a Paediatric Endocrinology Clinic.

Ghassan Faisal Fadlalbari, Renson O Mukhwana, Mohamed Ahmed Abdullah

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Frequent Collaborators

4 joint publications

Mohamed A Abdullah

3 joint publications

Salwa A Musa

3 joint publications

Samar S Hassan

2 joint publications

Elisa De Franco