Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Mahmoud Al-Sheyyab"'
Autor:
Ahmed H. Al Sharie, Yazan O. Al Zu'bi, Balqis M. Abu Mousa, Sohaib Al Khatib, Mahmoud Al-Sheyyab, Eyad Altamimi
Publikováno v:
Human Gene. 36:201171
Autor:
Jean Francois Baladi, Chang-Gong Liu, Paola Piccioni, Byung Woog Kang, Joon Ho Moon, Sule Menziletoglu Yildiz, Miyuki Tsutsui, Safak Ersoz, B. Girolami, Hidenori Imai, Mehmet Arslan, Norio Komatsu, Sang Kyun Sohn, Giampaolo Talamo, Paolo Vigneri, Yu Yang, Nunziatina Laura Parrinello, Kusai Al Zir, Vittorio Del Fabro, S. Marun, Faris A. Ahmed, Thomas P. Loughran, Jocelyn L. Wozney, Shahina Daar, Reinhold Munker, Yasushi Isobe, Cristian Taccioli, Mariangela Palladino, Mahmoud Al-Sheyyab, Simona Sica, Ali T. Taher, Fabio Stagno, Anna Triolo, Hiroko Suto, Francesco Di Raimondo, Shi-Nae Kim, Idanna Innocenti, Hansjuerg Alder, Dany Habr, Amal El-Beshlawy, Ulrike Kriemler-Krahn, I. Bertozzi, Maurizio Zangari, Yee Soo Chae, Abdulla A. Damluji, A. Girolami, Makoto Sasaki, Inci Akyuzluer, Patrizia Chiusolo, Diana Rofail, Murat Erkut, Nyla A. Heerema, E. Allemand, Giuseppe Leone, Abdullah Al Jefri, Mohsen Saleh Elalfy, Federica Sorà, Suleyman Dincer, Jong Gwang Kim, Kazuo Oshimi, Tatyana Feldman, Michela Tarnani, Suleimman A. Al-Sweedan, Hashem Jaddou, Pritish K. Bhattacharyya, Luca Laurenti, Hajime Yasuda, Secaatin Okten, N. Candeo, Birol Guvenc, Xiao Yan Yang, Mohammed Mueen, Nergiz Erkut, Ferda Tekinturhan, Tao Hong, Mehmet Sönmez, Koichi Sugimoto, Hailing Zhang, Dong-Zhi Li, Hakan Erkman
Publikováno v:
Acta Haematologica. 123:I-IV
Publikováno v:
Annals of Saudi Medicine, Vol 23, Iss 5, Pp 260-3 (2003)
BACKGROUND: Marked variations in the incidence of particular types of childhood cancer exist between countries. We report on the geographic variation in the occurrence of childhood cancer in Jordan. MATERIAL AND METHODS: Cases were identified from th
Publikováno v:
Journal of Tropical Pediatrics. 47:239-242
All patients presenting with hereditary hemolytic anemia, (n = 143) over a period of 18 months were enrolled in a study to evaluate the prevalence of hepatitis B, hepatitis C and HIV in multi-transfused patients in Jordan, and to identify possible re
Autor:
Mahmoud Al-Sheyyab, Azmi Hadidi, Nadim Jarrah, Kamel Ajlouni, Hatem El-Shanti, Abdulla S. Awidi, Mustafa M. Shennak, Enas Younis
Publikováno v:
European Journal of Pediatrics. 160:243-246
Wolfram syndrome (WS) is a recessively inherited disorder associated with recognised clinical features. Bleeding tendency was noticed in some of our patients, although this has not been reported before. We therefore studied this problem in all our WS
Publikováno v:
Annals of Tropical Paediatrics. 16:249-253
Homozygous sickle cell anaemia (SCA) is an inherited red blood cell disorder in which haemoglobin A is replaced by haemoglobin S. The disease exhibits a wide spectrum of clinical behaviour which has been well described in neighbouring countries. In J
Publikováno v:
Pediatric Hematology and Oncology. 10:119-128
The excretion of retinol-binding protein in early morning urine samples, expressed as a ratio to urinary creatinine (RBPCR), was used as a measure of proximal renal tubular toxicity in children during or after treatment with ifosfamide-containing che
Publikováno v:
Acta haematologica. 123(4)
Background: Protein C (PC) with its cofactor free protein S (FPS) are important anticoagulants. Any defect in the PC system is a risk factor for venous thrombosis. Aims: To assess the effect of intensity of smoking, and the dose-response for the numb
Publikováno v:
Tropical Doctor. 30:25-27
A prospective study of 203 children admitted with a first febrile seizure was carried out over 18 months. Aseptic meningitis was diagnosed in nine children (4%). The mean age of the children was 19.9 months and the peak age incidence (88%) was betwee
Publikováno v:
Annals of Tropical Paediatrics. 19:253-255
A prospective, matched, case-control study conducted over a period of 3 years was designed to examine the association of group A beta-haemolytic streptococcal infections and Henoch-Schonlein purpura. Demographic and clinical data were collected as we