Phenotype of apoptotic lymphocytes in children with Down syndrome

por Elsayed, Solaf M, Elsayed, Ghada M
Publicado 2009

Cholestasis in patients with Cockayne syndrome and suggested modified criteria for clinical diagnosis

por Abdel Ghaffar, Tawhida Y, Elsobky, Ezzat S, Elsayed, Solaf M
Publicado 2011

Orthopaedic manifestations of Proteus syndrome in a child with literature update()

por EL-Sobky, Tamer Ahmed, Elsayed, Solaf M., EL Mikkawy, Dalia M.E.
Publicado 2015

A case of infantile osteopetrosis: The radioclinical features with literature update()

por EL-Sobky, Tamer Ahmed, Elsobky, Ezzat, Sadek, Ismaiel, Elsayed, Solaf M., Khattab, Mohamed Fawzy
Publicado 2015

Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations

por Elsebaie, Hanan, Mansour, Mohamed Abdelhafiz, Elsayed, Solaf M., Mahmoud, Shady, El-Sobky, Tamer A.
Publicado 2021

Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients

por Abdel Ghaffar, Tawhida Y, Elsayed, Solaf M, Elnaghy, Suzan, Shadeed, Ahmed, Elsobky, Ezzat S, Schmidt, Hartmut
Publicado 2011

Extra-hepatic portal vein thrombosis in children: Single center experience

por Abdel-Ghaffar, Tawhida Yassin, Zakaria, Haidy Mohammed, Naghi, Suzan El, Elsayed, Solaf M, Haseeb, Alaa, Sobhy, Gihan Ahmed
Publicado 2023

MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature

por Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.
Publicado 2020

The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care

por Wilson, Brian T., Stark, Zornitza, Sutton, Ruth E., Danda, Sumita, Ekbote, Alka V., Elsayed, Solaf M., Gibson, Louise, Goodship, Judith A., Jackson, Andrew P., Keng, Wee Teik, King, Mary D., McCann, Emma, Motojima, Toshino, Murray, Jennifer E., Omata, Taku, Pilz, Daniela, Pope, Kate, Sugita, Katsuo, White, Susan M., Wilson, Ian J.
Publicado 2016

Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read...

por Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Müller‐Hofstede, Cornelie, Charbel Issa, Peter, Heller, Raoul, Beck, Bodo, Rüther, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M., Huhle, Dagmar, Elsayed, Solaf M., Taha, Hesham M., Baig, Shahid M., Stöhr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Nagel‐Wolfrum, Kerstin, Khan, Arif O., Bolz, Hanno J.
Publicado 2017

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

por Almeida, Ligia S., Pereira, Catarina, Aanicai, Ruxandra, Schröder, Sabine, Bochinski, Tomasz, Kaune, Anett, Urzi, Alice, Spohr, Tania C. L. S., Viceconte, Nikenza, Oppermann, Sebastian, Alasel, Mohammed, Ebadat, Saeedeh, Iftikhar, Sana, Jasinge, Eresha, Elsayed, Solaf M., Tomoum, Hoda, Marzouk, Iman, Jalan, Anil B., Cerkauskaite, Agne, Cerkauskiene, Rimante, Tkemaladze, Tinatin, Nadeem, Anjum Muhammad, El Din Mahmoud, Iman Gamal, Mossad, Fawzia Amer, Kamel, Mona, Selim, Laila Abdel, Cheema, Huma Arshad, Paknia, Omid, Cozma, Claudia, Juaristi-Manrique, Carlos, Guatibonza-Moreno, Pilar, Böttcher, Tobias, Vogel, Florian, Pinto-Basto, Jorge, Bertoli-Avella, Aida, Bauer, Peter
Publicado 2022