Search Results - "El‐Karaksy, H."

Hypermanganesemia with dystonia, polycythemia and cirrhosis in 10 patients: Six novel SLC30A10 mutations and further phenotype delineation by Zaki, M.S., Issa, M.Y., Elbendary, H.M., El‐Karaksy, H., Hosny, H., Ghobrial, C., El Safty, A., El‐Hennawy, A., Oraby, A., Selim, L., Abdel‐Hamid, M.S.

“…Biallelic mutations in the SLC30A10 gene cause an inborn error of Mn metabolism characterized by hypermanganesemia, polycythemia, early‐onset dystonia, and…”
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Prevalence and risk factors of asymptomatic hepatitis C virus infection in Egyptian children by MS EI-Raziky M EI-Hawary G Esmat AM Abouzied N EI-Koofy N Mohsen S Mansour A Shaheen M Abdel Hamid H EI-Karaksy

“…AIM： To identify the prevalence, risk factors and manifestations of asymptomatic hepatitis C virus （HCV） infection in Egyptian children. METHODS： Children at…”
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Anti-HCV prevalence among diabetic and non-diabetic Egyptian children by El-Karaksy, H, Anwar, G H, El-Raziky, M S, El-Hawary, M, Hashem, M, El-Sayed, R, El-Shabrawi, M, Mohsen, N, Fouad, H, Esmat, G

“…Our aim was to determine the prevalence of the HCV infection among children with type 1 DM as compared to a group of non-diabetic children attending the…”
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Hepatitis C virus infection in Egyptian children: single centre experience by El-Raziky, M. S., El-Hawary, M., El-Koofy, N., Okasha, S., Kotb, M., Salama, K., Esmat, G., El-Raziky, M., Abouzied, A. M., El-Karaksy, H.

“…The outcome of hepatitis C virus (HCV) infection acquired in childhood is uncertain because of the diversity of the epidemiological and clinical features of…”
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A challenging case of hereditary type 1 tyrosinaemia associated with persistent diarrhoea: Case report and literature review by Yassin, N A, Mogahed, E A, El-Karaksy, H

“…Hereditary tyrosinaemia type 1 (HT1) is a rare inherited genetic disorder attributed to deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). HT1 may…”
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A challenging case of hereditary type 1 tyrosinaemia associated with persistent diarrhoea : case report and literature review by Mogahed, E.A., Yassin, N.A., El-Karaksy, H.

“…Hereditary tyrosinaemia type 1 (HT1) is a rare inherited genetic disorder attributed to deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). HT1 may…”
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Post-portoenterostomy triangular cord sign prognostic value in biliary atresia : a prospective study by KOTB, M. A, SHEBA, M, EL KOOFY, N, MANSOUR, S, EL KARAKSY, H. M, DESSOUKI, N. M, MOSTAFA, W, EL BARBARY, M, EL-TANTAWY, H. E, KADDAH, S

“…The triangular cord sign (TC sign) is a sensitive and specific tool in prompt diagnosis of extrahepatic biliary atresia. The objective of this study is to…”
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P417 WILSON DISEASE ATP7B GENE MUTATIONS IN EGYPTIAN CHILDREN: REPORT OF TWO NOVEL MUTATIONS by El-Mougy, F, Sharaf, S, Elsharkawy, M, Mandour, I, Elessawy, R, Eldin, A, Helmy, H, Soliman, D, Hussein, L, Sharafeldin, H, Adel, E, El-Karaksy, H

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611 HEPATIC IMPAIRMENT IN EGYPTIAN CHILDREN WITH TYPE 1 DIABETES MELLITUS by El-Karaksy, H, Anwar, G, Mansour, S, El-Koofy, N, El-Sayed, R, Helmy, H, Mina, H, Sabry, M, Esmat, G

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Evaluation of the Triangular Cord Sign in the Diagnosis of Biliary Atresia by Kotb, Magd A, Kotb, Ahmed, Sheba, Maha F, Koofy, Nehal M. El, El-Karaksy, Hanaa M, Abdel-Kahlik, Mohamed K, Abdalla, Ahmed, El-Regal, Mohammed Ez, Warda, Rady, Mostafa, Hosam, Karjoo, Manoochehr, A-Kader, Hassan H

“…Infantile cholestasis continues to represent a diagnostic challenge. It is very important to diagnose surgically correctable disorders, such as biliary…”
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Capillaria philippinensis: A Cause of Fatal Diarrhea in One of Two Infected Egyptian Sisters by El-Karaksy, Hanaa, El-Shabrawi, Mortada, Mohsen, Nabil, Kotb, Magd, El-Koofy, Nehal, El-Deeb, Nadia

“…Capillaria philippinensis is an emerging infection in Egypt. Reports in children are scarce. We report here two sisters with C. philippinensis infection, aged…”
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Human fascioliasis in Egyptian children: successful treatment with triclabendazole by El-Karaksy, H, Hassanein, B, Okasha, S, Behairy, B, Gadallah, I

“…Human fascioliasis (HF) is an increasingly recognized public health problem in Egypt. During the past two years we diagnosed HF in 40 Egyptian children…”
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Diagnosis and management of galactosemia: an Egyptian experience by Fateen, E, el-Shafei, S, el-Karaksy, H, Mahmoud, M, Roshdy, S, el-Temtamy, S, Shin, Y

“…To screen normal and high risk Egyptian neonates for galactosemia. The study included 2238 neonates classified into two groups. Group I included screening of…”
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Celiac Disease in Children and Adolescents with Autoimmune Hepatitis: a Single-centre Experience by EI-SHABRAWI, Mortada, EL-KARAKSY, Hanaa, MOHSEN, Nabil, ISA, Mona, AL-BILTAGI, Mohammed, EL-ANSARI, Mervat

“…Celiac disease (CD) is increasingly reported from North Africa, including Egypt. Autoimmune hepatitis (AIH) is considered a high risk factor for CD. We aimed…”
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A child with rotor syndrome and Capillaria philippinensis: case report and review of literature by Helmy, H, El-Dib, N, Mogahed, E, Yasin, N, El-Karaksy, H

“…This paper reported Capillaria philippinensis in an Egyptian child based on clinical and laboratory diagnosis. The patient was successfullly treated with…”
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Human Fascioliasis: Clinical Features and Diagnostic Difficulties in Egyptian Children by El-Shabrawi, M., El-Karaksy, H., Okasha, S., El-Hennawy, A.

“…Human fascioliasis (HF) has been reported in children worldwide and occasionally from Egypt. In the past 7 years we diagnosed 16 children aged 3.5–11 years…”
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Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study by El-Karaksy, Hanaa, El-Koofy, Nehal, El-Hawary, Manal, Mostafa, Azza, Aziz, Mona, El-Shabrawi, Mortada, Mohsen, Nabil A, Kotb, Magd, El-Raziky, Mona, El-Sonoon, Marwa Abu, A-Kader, Hassan

“…No identifiable cause can be found in more than half of the cases of portal vein thrombosis (PVT). Our aim was to assess the prevalence of factor V Leiden…”
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Cost-effectiveness of prescreening versus empirical vaccination for hepatitis A in Egyptian children with chronic liver disease/Rapport cout-efficacite du predepistage compare a la methode empirique de vaccination contre l'hepatite A chez des enfants egyptiens souffrant d'une affection hepatique chronique by El-Karaksy, H, El-Sayed, R, El-Raziky, M, El-Koofy, N, Mansour, S

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Cost-effectiveness of prescreening versus empirical vaccination for hepatitis A in Egyptian children with chronic liver disease by El-Karaksy, H, El-Sayed, R, El-Raziky, M, El-Koofy, N, Mansour, S

“…The aim of the study was to determine the prevalence of anti-hepatitis A virus (anti-HAV) antibodies among 172 children with chronic liver disease, and to…”
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Is biliary atresia an autoimmune disease? by A-Kader, Hassan H, Abdel-Hameed, Ahmed, Al-Shabrawi, Mortada, Mohsen, Nabil, El-Karaksy, Hanaa, Hassanein, Bahaa, Elsayed, Behairy, Abdel-Khalik, Mohammed K, Karjoo, Manoochehr

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