Neveen A Soliman

11PUBLICATIONS
37CO-AUTHORS
Gene mappingDevelopmental genetics (incl. sex determination)Medical devicesInfant and child healthNeurology and neuromuscular diseases
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Publications (11)

|May 22, 2025
Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndrome.

Neveen A Soliman, Mohamed A Elmonem, Ahmed F El-Sayed

|Oct 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndrome.

Karim Karimi, Denisa Weis, Ingvild Aukrust

|May 20, 2022
Primary hyperoxaluria type 1 in developing countries: novel challenges in a new therapeutic era.

Neveen A Soliman, Sameh Mabrouk

|Apr 12, 2022
Newborn Screening: Review of its Impact for Cystinosis.

Katharina Hohenfellner, Ewa Elenberg, Gema Ariceta

|Nov 18, 2021
Clinical and neurophysiological characterization of early neuromuscular involvement in children and adolescents with nephropathic cystinosis.

Nour Elkhateeb, Rasha Selim, Neveen A Soliman

|Feb 01, 2021
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice.

Amar J Majmundar, Florian Buerger, Thomas A Forbes

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Frequent Collaborators

2 joint publications

Khaled Amer

2 joint publications

Mohamed A Elmonem

2 joint publications

Friedhelm Hildebrandt

1 joint publications

Sofia Douzgou Houge