Works by Wahba, Yahya

Results: 27

Shone᾽s complex in pediatric age group: clinical characteristics, structural components, interventions, and outcomes of a cohort from a single center.

Published in:

BMC Pediatrics, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12887-025-05716-3

By:

Rakha, Shaimaa;
Ali, Marwa Said;
El Derie, Ahmad Abd El Aleem;
Wahba, Yahya;
Elkheir, Mohammed Magdy Abo

Publication type:

Article

Lymphocyte subgroups and recurrent infections in children with Down syndrome – a prospective case control study.

Published in:

Central European Journal of Immunology, 2018, v. 43, n. 3, p. 248, doi. 10.5114/ceji.2018.80042

By:

MITWALLI, MAHA;
WAHBA, YAHYA;
SHALTOUT, ALI;
GOUIDA, MONA

Publication type:

Article

Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H-syndrome.

Published in:

Pediatric Diabetes, 2015, v. 16, n. 4, p. 305, doi. 10.1111/pedi.12160

By:

Al‐Haggar, Mohammad;
Salem, Nanees;
Wahba, Yahya;
Ahmad, Nermin;
Jonard, Laurence;
Abdel‐Hady, Dina;
El‐Hawary, Amany;
El‐Sharkawy, Ashraf;
Eid, Abdel‐Rhman;
El‐Hawary, Amira

Publication type:

Article

Effects of Cerebrolysin on the Neurodevelopmental Outcomes in Infants with Down Syndrome: A Randomized Controlled Pilot Trial.

Published in:

Journal of Mental Health Research in Intellectual Disabilities, 2022, v. 15, n. 4, p. 306, doi. 10.1080/19315864.2022.2098433

By:

Salah El-Din, Ahmed;
Yahia, Sohier;
Zeid, Mayada Sabry;
El-Hadidy, Mohamed Adel;
Wahba, Yahya

Publication type:

Article

Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations.

Published in:

Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 71, doi. 10.1097/01.MXE.0000414810.01450.3c

By:

Al-Haggar, Mohammad;
Taranta, Anna;
El-Hawary, Amany;
Al-Said, Afaf;
Shaban, Abdel-Aziz;
Wahba, Yahya

Publication type:

Article

Evaluation of serum levels of interferon beta (INF-B) and Nucleotide-binding oligomerization domain 2 (NOD2) gene polymorphism in children with atopic asthma phenotype.

Published in:

Alexandria Journal of Pediatrics, 2023, v. 36, n. 2, p. 113, doi. 10.4103/ajop.ajop_25_23

By:

Zedan, Magdy M. E.;
Aloraby, Rania S.;
Abousamra, Nashwa K.;
Wahba, Yahya;
Abd El-Hameed, Suzy A. El-Mabood

Publication type:

Article

CD40 and CD72 expression and prognostic values among children with systemic lupus erythematosus: a case–control study.

Published in:

Lupus, 2020, v. 29, n. 10, p. 1270, doi. 10.1177/0961203320941931

By:

Asmiyou, Abtisam;
Bakr, Ashraf M;
Shahin, Doaa A;
Wahba, Yahya

Publication type:

Article

Oxidative stress and vitamin D receptor BsmI gene polymorphism in Egyptian children with systemic lupus erythematosus: a single center study.

Published in:

Lupus, 2019, v. 28, n. 6, p. 771, doi. 10.1177/0961203319846380

By:

Fouad, Hend;
Yahia, Sohier;
Elsaid, Afaf;
Hammad, Ayman;
Wahba, Yahya;
El-Gilany, Abdel-Hady;
Abdel-Aziz, Abdel -Aziz Fatouh

Publication type:

Article

Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution's 5-year experience.

Published in:

Middle East Fertility Society Journal, 2022, v. 27, n. 1, p. 1, doi. 10.1186/s43043-022-00101-x

By:

El-Dahtory, Faeza;
Yahia, Sohier;
Rasheed, Rabab Ahmed;
Wahba, Yahya

Publication type:

Article

Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution’s 5-year experience.

Published in:

Middle East Fertility Society Journal, 2022, v. 27, n. 1, p. 1, doi. 10.1186/s43043-022-00101-x

By:

El-Dahtory, Faeza;
Yahia, Sohier;
Rasheed, Rabab Ahmed;
Wahba, Yahya

Publication type:

Article

CYP2C9 (2&3) and CYP2C19 (2&3) polymorphisms among children with nonlesional epilepsy: a single-center study.

Published in:

Acta Neurologica Belgica, 2021, v. 121, n. 6, p. 1623, doi. 10.1007/s13760-020-01442-y

By:

Eltalal, Samah;
El Ayouty, Mostafa;
El-Said, Afaf;
Wahba, Yahya

Publication type:

Article

Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study.

Published in:

2017

By:

El-Gilany, Abdel-Hady;
Yahia, Sohier;
Wahba, Yahya

Publication type:

journal article

Disruptive behavior in Down syndrome children: a cross-sectional comparative study.

Published in:

Annals of Saudi Medicine, 2014, v. 34, n. 6, p. 517, doi. 10.5144/0256-4947.2014.517

By:

Yahia, Sohier;
El-Hadidy, Mohamed;
El-Gilany, Abdel-Hady;
Amdel-Hady, Dina;
Wahba, Yahya;
Al-Haggar, Mohammad

Publication type:

Article

Sporadic Fiibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature.

Published in:

Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/834605

By:

Al-Haggar, Mohammad;
Ahmad, Nermin;
Yahia, Sohier;
Shams, Amany;
Hasaneen, Bothina;
Hassan, Rasha Hassan;
Wahba, Yahya;
Salem, Nanees Abdel-Badie;
Abdel-Hady, Dina

Publication type:

Article

Burden of family caregivers of Down syndrome children: a cross-sectional study.

Published in:

2021

By:

El-Deen, Nadia Alam;
Alwakeel, Angi A;
El-Gilany, Abdel-Hady;
Wahba, Yahya;
Alam El-Deen, Nadia

Publication type:

journal article

Prevalence of Helicobacter pylori infection among children with primary nephrotic syndrome: a cross-sectional study.

Published in:

African Health Sciences, 2020, v. 20, n. 4, p. 1624, doi. 10.4314/ahs.v20i4.15

By:

Mahmoud, Ahmed;
Bakr, Ashraf;
Elsaid, Afaf;
Wahba, Yahya

Publication type:

Article

A Novel Fibrillin–1 Mutation in an Egyptian Marfan Family: A Proband Showing Nephrotic Syndrome Due to Focal Segmental Glomerulosclerosis.

Published in:

Saudi Journal of Kidney Diseases & Transplantation, 2017, v. 28, n. 1, p. 141, doi. 10.4103/1319-2442.198166

By:

Al-Haggar, Mohammad;
Bakr, Ashraf;
Wahba, Yahya;
Coucke, Paul J.;
El-Hussini, Fatma;
Hafez, Mona;
Eid, Riham;
Eid, Abdel-Rahman;
Sarhan, Amr;
Shaltout, Ali;
Hammad, Ayman;
Yahia, Sohier;
El-Rifaie, Ahmad;
Abdel-Hadi, Dina

Publication type:

Article

Comparison of Soybean-based Oil and MCT-olive-fish-soy Oil Intravenous Lipid Emulsions on Soluble Adhesion Markers in Preterm Neonates with Sepsis: A Randomized Controlled Trial.

Published in:

Indian Pediatrics, 2019, v. 56, n. 10, p. 841, doi. 10.1007/s13312-019-1610-7

By:

Abdelkareem, Mohammed;
Wahba, Yahya;
Shouman, Basma;
Mesbah, Abeer

Publication type:

Article

Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.

Published in:

Clinical & Experimental Nephrology, 2012, v. 16, n. 4, p. 604, doi. 10.1007/s10157-012-0603-9

By:

Al-Haggar, Mohammad;
Sakamoto, Osamu;
Shaltout, Ali;
Al-Hawari, Amani;
Wahba, Yahya;
Abdel-Hadi, Dina

Publication type:

Article

Evaluation of the left ventricular systolic strain in hypocalcemic infants with two‐dimensional speckle tracking echocardiography.

Published in:

Echocardiography, 2022, v. 39, n. 4, p. 568, doi. 10.1111/echo.15329

By:

Aboelata, Shaimaa;
Elmarsafawy, Hala;
Atwa, Mohamed A.;
Wahba, Yahya

Publication type:

Article

Genetic and biochemical studies of hepatic carcinoma in the Egyptian population.

Published in:

Journal of Research in Medical Sciences, 2021, p. 1, doi. 10.4103/jrms.JRMS_846_17

By:

Elkhoudary, Amany F.;
Elmougy, Rehab;
Elsaid, Afaf;
Wahba, Yahya;
Abdel-Aziz, Abdel-Aziz F.

Publication type:

Article

Polymorphisms of the sodium voltage-gated channel, alpha subunit 1 (SCN1A -A3184G) gene among children with non-lesional epilepsy: a case-control study.

Published in:

Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01350-2

By:

Ghazala, Esraa;
Shahin, Doaa A.;
Wahba, Yahya

Publication type:

Article

Prevalence and CCR3-T51C genotype–phenotype correlation of bronchial asthma among basic education school children: an observational study.

Published in:

Egyptian Pediatric Association Gazette, 2024, v. 72, n. 1, p. 1, doi. 10.1186/s43054-024-00306-x

By:

Zedan, Magdy;
Elwassefy, Mona;
Zareif, Ismail El;
ElTahan, Hossam;
Wahba, Yahya

Publication type:

Article

Evaluation of serum levels of interferon beta and nucleotide binding and oligomerization domain 2 gene polymorphism in children with cough asthma phenotype: a case–control study.

Published in:

Egyptian Pediatric Association Gazette, 2023, v. 71, n. 1, p. 1, doi. 10.1186/s43054-023-00183-w

By:

Zedan, Magdy M.;
Radwan, Doaa M.;
Abousamra, Nashwa Khairat;
Wahba, Yahya Mohammed;
Osman, Engy

Publication type:

Article

Camurati-Engelmann disease: New clinical insights in an Egyptian case report.

Published in:

2020

By:

Wahba, Yahya;
Abdel Ghaffar, Nevert A.;
Shaltout, Ali;
Elsharkawy, Ashraf

Publication type:

journal article

Rapunzel syndrome (gastric trichobezoar), a rare presentation with generalised oedema: case report and review of the literature.

Published in:

Paediatrics & International Child Health, 2019, v. 39, n. 1, p. 76, doi. 10.1080/20469047.2017.1389809

By:

Nour, Islam;
Abd Alatef, Mona;
Megahed, Ahmed;
Yahia, Sohier;
Wahba, Yahya;
Shabaan, Abd Elazeez

Publication type:

Article

Neurocutaneous melanosis is not always a benign disease.

Published in:

2020

By:

El Mabood, Suzy Abd;
Wahba, Yahya;
Yahia, Sohier;
Sarhan, Mohammed M;
Mansour, Ahmed K;
Provenzano, Aldesia;
Elmahdi, Hoda S;
Darwish, Ahmad

Publication type:

Case Study