Search Results - "Rimawi, Hala"

A rare case of Evans syndrome associated with sudden loss of vision: A case report by Ababneh, Laila T, Mahmoud, Ikhlas H, Al-Rimawi, Hala S

“…Purpose: To report a case of Evans syndrome with a vascular occlusive event leading to severe loss of vision. Case report: A 12-year-old boy with Evans…”
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Idiopathic Hypertrophic Pachymeningitis in a Child With Hydrocephalus by Aburahma, Samah K., MD, Anabtawi, Abdel Ghani M., MD, Al Rimawi, Hala S., MD, Elheis, Mwaffaq A., MD, Mohtaseb, Aliaa H., MD

“…Idiopathic hypertrophic pachymeningitis is a rare but increasingly recognized disorder characterized by diffuse thickening of the dura mater of unknown…”
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Dental discoloration: an overview by Hattab, F N, Qudeimat, M A, al-Rimawi, H S

“…Often the first evidence of variation from normal in human dentition is an observable difference in the color of the teeth. During the past decade, the demand…”
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Intrauterine upper limb ischemia associated with fetal thrombophilia: a case report and review of the literature by Khriesat, Wadah M, Al-Rimawi, Hala S, Lataifeh, Isam M, Al-Sweedan, Suleimman, Baqain, Eyad

“…Neonatal extremity gangrene is rare, even rarer are those born with evidence of intrauterine vascular occlusion. Intrauterine limb ischemia has been attributed…”
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Emergency peripartum hysterectomy in Northern Jordan: indications and obstetric outcome (an 8-year review) by El-Jallad, Mohammad Fayez, Zayed, Faheem, Al-Rimawi, Hala S

“…To review cases of emergency peripartum hysterectomy regarding their incidence, risk factors, indications and complications and their results were carefully…”
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Predictors of severe hemolysis in patients with glucose-6-phosphate dehydrogenase deficiency following exposure to oxidant stresses by Al-Sweedan, Suleimman A, Jdaitawi, Hussein, Khriesat, Wadah M, Khader, Yousef Y, Al-Rimawi, Hala S

“…BACKGROUND AND OBJECTIVES Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic enzymatic disorder that affects millions of people worldwide, and is…”
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Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium by Bakry, Doua, Aronson, Melyssa, Durno, Carol, Rimawi, Hala, Farah, Roula, Alharbi, Qasim Kholaif, Alharbi, Musa, Shamvil, Ashraf, Ben-Shachar, Shay, Mistry, Matthew, Constantini, Shlomi, Dvir, Rina, Qaddoumi, Ibrahim, Gallinger, Steven, Lerner-Ellis, Jordan, Pollett, Aaron, Stephens, Derek, Kelies, Steve, Chao, Elizabeth, Malkin, David, Bouffet, Eric, Hawkins, Cynthia, Tabori, Uri

“…Abstract Background Constitutional mismatch repair deficiency (CMMRD) is a devastating cancer predisposition syndrome for which data regarding clinical…”
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Efficacy, Safety, and Biomarker Analysis of 5 Mg and 7.5 Mg Doses of Crizanlizumab in Patients with Sickle Cell Disease: Primary Analyses from the Phase III STAND Study by Abboud, Miguel R, Cançado, Rodolfo D, De Montalembert, Mariane, Smith, Wally R, Rimawi, Hala, Voskaridou, Ersi, Guvenc, Birol, Keefe, Deborah, Grosch, Kai, Nassin, Michele L, Watson, Jimmy, Yssel, Justin, Reshetnyak, Evgeniya, Adomakoh, Yvonne Dei

“…Background: Crizanlizumab, a selective, humanized immunoglobulin G2 kappa anti-P-selectin monoclonal antibody, demonstrated positive clinical activity and…”
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Pediatric oncology situation analysis (Jordan) by Al-Rimawi, Hala Saleh

“…This article highlights the current situation of pediatric oncology in Jordan by reviewing the available population based data from the surveillance. Cancer…”
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Impact of treatment regimen with moroctocog alfa (AF‐CC) on bleeding rates in paediatric patients with severe haemophilia A by Smith, Mark P., Rupon, Jeremy, Wali, Yasser, Rimawi, Hala, Korth‐Bradley, Joan, Smith, Lynne, Rendo, Pablo

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Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium by Aronson, Melyssa, Gallinger, Steven, Cohen, Zane, Cohen, Shlomi, Dvir, Rina, Elhasid, Ronit, Baris, Hagit N, Kariv, Revital, Druker, Harriet, Chan, Helen, Ling, Simon C, Kortan, Paul, Holter, Spring, Semotiuk, Kara, Malkin, David, Farah, Roula, Sayad, Alain, Heald, Brandie, Kalady, Matthew F, Penney, Lynette S, Rideout, Andrea L, Rashid, Mohsin, Hasadsri, Linda, Pichurin, Pavel, Riegert-Johnson, Douglas, Campbell, Brittany, Bakry, Doua, Al-Rimawi, Hala, Alharbi, Qasim Kholaif, Alharbi, Musa, Shamvil, Ashraf, Tabori, Uri, Durno, Carol

“…Hereditary biallelic mismatch repair deficiency (BMMRD) is caused by biallelic mutations in the mismatch repair (MMR) genes and manifests features of…”
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Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study by Karimi, Mehran, Zarei, Tahereh, Haghpanah, Sezaneh, Azarkeivan, Azita, Kattamis, Christos, Ladis, Vassilis, Kattamis, Antonios, Kilinc, Yurdanur, Daar, Shahina, Alyaarubi, Saif, Khater, Doaa, Wali, Yasser, Elshinawy, Mohamed, Almadhani, Ali, Yassin, Mohamed, Soliman, Ashraf T., Canatan, Duran, Obiedat, Maha, Al-Rimawi, Hala, Mariannis, Demetris, Christodoulides, Constantinos, Christou, Soteroula, Tzoulis, Ploutarchos, Campisi, Saveria, Di Maio, Salvatore, De Sanctis, Vincenzo

“…Background Data on the prevalence and type of endocrine disorders in β-thalassemia intermedia (β-TI) patients are scarce. This multicenter study was designed…”
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Sport participation in adolescents with sickle cell disease by Al-Rimawi, Hala, Jallad, Samer

“…Adolescents with blood diseases should be encouraged to participate in exercise. Physical activity helps to build stronger muscles, to give better support to…”
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An ICET- A survey on Hypoparathyroidism in Patients with Thalassaemia Major and Intermedia: A preliminary report by De Sanctis, Vincenzo, Soliman, Ashraf T, Canatan, Duran, Elsedfy, Heba, Karimi, Mehran, Daar, Shahina, Rimawi, Hala, Christou, Soteroula, Skordis, Nicos, Tzoulis, Ploutarchos, Sobti, Praveen, Kakkar, Shruti, Kilinc, Yurdanur, Khater, Doaa, Alyaarubi, Saif A, Kaleva, Valeriya, Lum, Su Han, Yassin, Mohamed A, Saki, Forough, Obiedat, Maha, Anastasi, Salvatore, Galati, Maria Concetta, Raiola, Giuseppe, Campisi, Saveria, Soliman, Nada, Elshinawy, Mohamed, Jaouni, Soad Al, Di Maio, Salvatore, Wali, Yasser, Elhakim, Ihab Zaki, Kattamis, Christos

“…Hypoparathyroidism (HPT) is a rare disease with leading symptoms of hypocalcemia, associated with high serum phosphorus levels and absent or inappropriately…”
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MECC regional initiative in pediatric palliative care: Middle Eastern course on pain management by Silbermann, Michael, Al-Hadad, Salma, Ashraf, Shamvil, Hessissen, Laila, Madani, Abdellah, Noun, Peter, Khayat, Claudia, Al-Rimawi, Hala, Kebudi, Rejin, Yaniv, Isaac

“…In all the major medical centers throughout the Middle East, there is a functioning pediatric hematology oncology department. In almost all countries, opioids…”
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548 Gastrointestinal (GI) Findings in Patients With Biallelic Mismatch Repair (BMMRD) Gene Deficiency Syndrome: Report From the International Consortium by Durno, Carol, Aronson, Melyssa, Tabori, Uri, Gallinger, Steven, Cohen, Shlomi, Dvir, Rina, Elhasid, Ronit, Feldman, Hagit B, Druker, Harriet, Chan, Helen, Ling, Simon, Kortan, Paul P, Holter, Spring, Semotiuk, Kara, Malkin, David, Farah, Roula, Leach, Brandie, Kalady, Matthew F, Penney, Lynette S, Rideout, Andrea L, Rashid, Mohsin, Hasadsri, Linda, Pichurin, Pavel, Riegert-Johnson, Douglas, Campbell, Brittany, Bakry, Doua, Rimawi, Hala, Alharbi, Qasim K, Alharbi, Musa M, Ashraf, Shamvil, Kariv, Revital, Sayad, Alain, Cohen, Zane

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Mediterranean glucose-6-phosphate dehydrogenase (G6PD(C563T)) mutation among Jordanian females with acute hemolytic crisis by Al-Alimi, Abdullah Abdul Jabbar Ahmed, Kanakiri, Naeem, Kamil, Muhammad, Al-Rimawi, Hala Saleh, Zaki, Abdul Hamid, Yusoff, Narazah Mohammad

“…To evaluate the G6PD(C563T) Mediterranean mutation among Jordanian females who were admitted to Princess Rahma Teaching Hospital (PRTH) with/or previous…”
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Pubertal evaluation of adolescent boys with beta-thalassemia major and delayed puberty by Al-Rimawi, Hala Saleh, Jallad, Mohammad Fayez, Amarin, Zouhair Odeh, Al Sakaan, Rula

“…To examine the hormonal status of the hypothalamic-pituitary-gonadal axis in adolescent males with beta-thalassemia major. Controlled clinical study. Tertiary…”
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Psychosocial and Economic Study of Families with β Thalassemic Children in Northern Jordan by Sadiq, May F. G., Rimawi, Hala S., Haddad, Linda G.

“…Some aspects of β thalassemia major in Jordan were defined. The study included interviews with 77 out of 81 families with multi-transfused β thalassemia…”
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Dental discoloration: An overview by Hattab, Faiez N, Qudeimat, Muawia A, Al-Rimawi, Hala S

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