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                             59 results found
no title author magazine year volume issue page(s) type
1 Acquired Hemophilia: A Report on 2 Cases Saidi, Ghassen

18 6S p. S13
article
2 Activated Partial Thromboplastin Time Clot Waveform Analysis In Hemophilia A Said, Maha

18 6S p. S14
article
3 A descriptive study of patients with myelodysplastic syndrome: experience of the clinical hematology department of Monastir-Tunisia Cheffai, Arij

18 6S p. S19
article
4 Adverse effects of Imatinib in patients with chronic myeloid leukemia Masrour, Hajar

18 6S p. S15-S16
article
5 Allogeneic Hematopoietic Stem Cell Transplantation In Aplastic Anemia: Experience Of The Pediatric Hematology And Oncology Department In Rabat (Morocco) Lakhrissi, M.

18 6S p. S11
article
6 Assessing Bone Mineral Density in Sickle Cell Disease Patients & Correlation to Frequency of Admission – Prospective - Uni Center Study AL-ANSARI, Rehab Yusuf

18 6S p. S1
article
7 Assessment of peripheral blood CD26+ leukemic stem cells in CML Patients : a preliminary study Frikha, Rim

18 6S p. S12
article
8 BCL2 overexpression in diffuse large B-cell Lymphoma Masrour, Hajar

18 6S p. S6-S7
article
9 Bleeding disorders in heavy menstrual bleeding; Debunking myths and revealing facts Ayad, Alia Abdel Aziz

18 6S p. S13
article
10 Bleeding phenotype in hemophilia carriers : Tunisian center experience Ghali, Ons

18 6S p. S14
article
11 Cancer Treatment Outcomes in Pediatric Patients with Glucose-6-phosphate dehydrogenase (G6PD) Deficiency Alsenaini, Ghusun Issam

18 6S p. S10
article
12 Can Social Education Interventions Programs Decrease Incidence of Sickle Cell Anemia? A Success Story from Khaibar, Saudi Arabia. Zolaly, Mohammed

18 6S p. S7-S8
article
13 Case Series with Haemoglobin Hope in Egyptian Family Moustafa, Amal Zaghloul

18 6S p. S9
article
14 CD5 expression in diffuse large B-cell lymphoma Bouchnafati, Sanaa

18 6S p. S17
article
15 Changes in the Fibrinolytic System of Patients Infected with Severe Acute Respiratory Syndrome Coronavirus2 Abudouleh, Esra'a

18 6S p. S3
article
16 Charity Medical Care For Hemoglobinopathies At Madinah, Saudi Arabia Al Hawsawi, Zakaria

18 6S p. S19-S20
article
17 Circumcision in haemophilia Moroccan Protocol El Ansari, N.

18 6S p. S12
article
18 Coexistence of JAK2V617F and CALR mutation in Tunisian cohort with Philadelphia-negative chronic myeloproliferative neoplasms Elmahmoudi, Hejer

18 6S p. S9
article
19 Effect of Low Dose of Hydroxyurea in SCD Children with Arab-Indian phenotype- Local Experience Hussein, Zahra Jaber

18 6S p. S10
article
20 Epidemiological characteristics of congenital bleeding disorders in south Tunisia Charfi, Maha

18 6S p. S6
article
21 Epidemiological Pattern Of Childhood Cancer Treated At Private Dr Suliman Fakeeh Hospital, Jeddah City, Saudi Arabia And Their Outcome Khattab, Taha

18 6S p. S19
article
22 Epidemiologic study of hereditary bleeding disorders in Dubai, UAE :A single center experience Elsherif, Yasmine Tarek

18 6S p. S1-S2
article
23 Evaluation of safety and efficacy of Emicizumab prophylaxis in Egyptian pediatric patients with Hemophilia A: Single center experience Zakaria, Marwa

18 6S p. S4
article
24 Factor V Deficiency And Geroderma Osteodysplastic : In Case Report Isfaoun, Z.

18 6S p. S24-S25
article
25 Factor VIII Level in Mothers of Patients with Severe Hemophilia A and its Impact on Joint Status Ragab, Iman

18 6S p. S17-S18
article
26 Follow-Up Of Hemophiles And Management Of Complications Zaier, Monia

18 6S p. S13-S14
article
27 Glanzmann thrombasthenia: Genotype / phenotype correlation Tarawah, Ahmad M.

18 6S p. S21
article
28 Heavy Menstrual Bleeding Among Glanzmann Thrombasthenia Ladies, Single-Center Experience Tarawah, Ahmad

18 6S p. S8
article
29 High incidence of Intracranial haemorrhage in Egyptian children with hereditary afibrinogenaemia: A single center study Abdelwahab, Magy

18 6S p. S18
article
30 Hospitalizations for sickle cell disease in Qatif central hospital pediatric population ALDarwish, Mohammed

18 6S p. S22
article
31 Hydroxyurea utilization and dose optimization in children with sickle cell disease (SCD) Alotaibi, Nour

18 6S p. S20
article
32 Immunodeficiency in Children with Diamond Blackfan Anemia Ragab, Iman

18 6S p. S18-S19
article
33 Inhibitor in people living with hemophilia B severe : A four cases report Ons, Ghali

18 6S p. S15
article
34 Inhibitor in Von Willebrand disease: Two case reports Ons, Ghali

18 6S p. S14-S15
article
35 Insights into Philadelphia Chromosome-Positive ALL: A Retrospective Study Aya, Zaouali Dridi

18 6S p. S15
article
36 Iron Deficiency Anemia among Patients with Glanzmann's Thrombasthenia: Single Center Experience Tarawah, Renad

18 6S p. S24
article
37 Iron Intake Among Women with Eating Disorders Tarawah, Renad A.

18 6S p. S24
article
38 Labor And Delivery Outcomes Among Ladies With Glanzmann Thrombasthenia Tarawah, Raghad

18 6S p. S21-S22
article
39 Long term outcome of allogeneic stem cell transplantation for patients with Fanconi Anemia Malak, Khayati

18 6S p. S6
article
40 Multiplex-PCR is a useful and economical method to detect large exon deletions in severe hemophilia A in developing countries: Experience of Tunisia Elmahmoudi, Hejer

18 6S p. S4
article
41 myWBDR Application Users’ Satisfaction Thabet, L.

18 6S p. S10-S11
article
42 Neurological Complications in Children with Sickle Cell Disease at Qatif Central Hospital in Saudi Arabia Hussein, Zahra Jaber

18 6S p. S22
article
43 Observational, PRO study to Evaluate Quality of Life for Hemophilia patients on Emicizumab, KSA Single center study Kashari, Ohoud

18 6S p. S11-S12
article
44 Oral health status and the impact of Oral health promotion in Children& Adolescents with Bleeding Disorders Abdelhafez, Nayera H.K.

18 6S p. S3-S4
article
45 Overview of Sickle-cell disease management in the Pediatric Hematology and Oncology Center of Rabat (Morocco) El kababri, Maria

18 6S p. S23-S24
article
46 Patient Care Strategies for alloant-ibodies in Type 3 Von Willebrand Disease: A Southern Tunisia Perspective Mallek, Rahma

18 6S p. S5
article
47 Polycythemia Vera and associated risk factors Sirine, Ben Salem

18 6S p. S16
article
48 Prevalence Of Peripherally Inserted Central Catheter Thrombosis In Acute Leukemia Patients Aljohani, Sara

18 6S p. S23
article
49 Prevalence of Transfusion Transmissible Diseases Between Madinah Blood Bank Donors, Saudi Arabia Al-Mutairi, Abdullah Barrak

18 6S p. S20-S21
article
50 Red blood cell automated exchange (RBCX) transfusion in sickle cell children: A single center experience from Madinah, KSA. Nashat, Mohamed

18 6S p. S8-S9
article
51 Refractory diffuse large B-cell Lymphoma Masrour, Hajar

18 6S p. S7
article
52 Relapse after allogeneic haematopoietic stem cell transplantation in children with acute lymphoblastic leukemia Sabrine, Mekni

18 6S p. S16
article
53 Subclinical Atherosclerosis in Childhood Acute Lymphoblastic leukemia Survivors: a Tertiary Center Experience Sherief, Laila

18 6S p. S2
article
54 The Bulky mass in diffuse large B Cell Lymphoma: Prognostic impact? A treatment guiding factor? Masrour,

18 6S p. S17
article
55 The effect of different types of anemia on HbA1c levels in non-diabetics Alzahrani, Basil

18 6S p. S2
article
56 The Multidimensional Impact of Sickle Cell Disease in Children on Parents and Family Functioning: A Cross Sectional Study Alfayez, Raed Abdullah

18 6S p. S9-S10
article
57 The Perception of Pediatric Sickle Cell Anemia Patients’ Caregivers toward Bone Marrow Transplantation at NGHA Jeddah, Saudi Arabia Betar, Manar

18 6S p. S2-S3
article
58 The Role of Hydroxyurea on Growth in Children with SCD Alkashi, Zahrah Mohammed

18 6S p. S22-S23
article
59 Von Willebrand Disease laboratory diagnosis in a low middle income country GHALI, O.N.S.

18 6S p. S5
article
                             59 results found
 
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