Author(s): Marta Isabel Wolff Echeverri | Carolina Rivera Álvarez | Silvia Emelia Herrera Higuita | Mónica María Escobar Franco | Juan Carlos Wolff Idárraga

Atrial septal defect closure on cardiopulmonary bypass in a sickle cell anemia: Role of hydroxyurea and partial exchange transfusion

Author(s): Gosavi Kundan | Dash Sananta | Shah Bharat | Upasani C

Common hepatic duct perforation in a sickle cell disease child.

Author(s): Al-Malki Talal | Ibrahim Ashraf

Sickle cell disease in Saudi Arabia : the Asian haplotype. Reflections on a meeting at Hofuf, September 2003.

Author(s): Serjeant Graham | Serjeant Beryl

Differences between males and females in adult sickle cell pain crisis in eastern Saudi Arabia.

Author(s): Udezue E | Girshab Abdel

Acute chest syndrome in adult sickle cell disease in eastern Saudi Arabia.

Author(s): Al-Suleiman Ahmad | Aziz Gassan | Bagshia Mahamoud | El Liathi Saeed | Homrany Hassan

Acute fulminant cholestatic jaundice in sickle cell disease

Author(s): Al-Suleiman Ahmad | Bu-sobaih Jawad

Patterns of mortality in adult sickle cell disease in the Al-Hasa region of Saudi Arabia

Revision hip arthroplasty in sickle cell disease

Author(s): Kalacy Aydyner | Ozkan Cenk | Togrul Emre

Recurrent posterior reversible encephalopathy syndrome in a patient with sickle cell disease

Author(s): Parameswaran Bimal | Krishnan Pudukode | Al Dossary Jamila

Salmonella pyomyositis complicating sickle cell anemia: a case report

Author(s): Wong Vanessa | Lissack Maxine | Turmezei Tom | Maitland Jenny

Phytochemical and Antisickling Studies of the Leaves of Hymenocardia acida Tul (Euphorbiaceae)

Author(s): H. Ibrahim | F.S. Sani | B.H. Danladi | A.A. Ahmadu

Co-existince of Sickle Cell Disease and Hemidiaphragm Paralysis

Author(s): I.M. Melek | D. Duman | C. Babayigit | E. Gali

Major Artery Occlusion: a Rare Complication of Sickle Cell Disease

Author(s): Adnan Agha

Abnormal hemoglobin variants, ABO, and Rhesus blood group distribution among students in the Niger Delta of Nigeria

Author(s): O Erhabor | TC Adias | Z A Jeremiah | et al

An “acquired” hemoglobin J variant in a sickle cell disease patient

Author(s): Nawwar Swedan | Kathleen Nicol | Phylis Moder | Samir Kahwash

Membranoproliferative Glomerulonephritis in a Postpartum Woman With Sickle Cell Disease

Author(s): Tausif Zar | Jayapriya Krishnaswamy | Harold T Yamase | Wilner Samson

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

Sickle cell cholangiopathy: An endoscopic retrograde cholangiopancreatography evaluation

Author(s): Hussain Issa, Ali Al-Haddad, Ahmed Al-Salem

Intrahepatic Cholestasis in Sickle Cell Disease: A Case Report

Asthma in Sickle Cell Disease: Implications for Treatment

Author(s): Kathryn Blake | John Lima

Collapsing glomerulopathy in sickle cell disease: a case report

Author(s): Ramidi Ganga | Kurukumbi Mohan | Sealy Peter

Psychological complications of childhood chronic physical illness in Nigerian children and their mothers: the implication for developing pediatric liaison services

Author(s): Bakare Muideen | Omigbodun Olayinka | Kuteyi Olugbenga | Meremikwu Martin | Agomoh Ahamefule

Cell therapy of hip osteonecrosis with autologous bone marrow grafting

Author(s): Hernigou Philippe | Poignard Alexandre | Zilber Sebastien | Rouard Helene

Transfusiones en pacientes con pruebas de compatibilidad positivas y en aquellos con anemia hemolítica autoinmune Approach to transfusion support in patients with positive compatibility tests and in those with autoimmune hemolytic anemia

Author(s): Julián Miguel Aristizábal Aristizábal | José Domingo Torres

Adverse Effects of a Clinically Relevant Dose of Hydroxyurea Used for the Treatment of Sickle Cell Disease on Male Fertility Endpoints

Induction of endogenous γ-globin gene expression with decoy oligonucleotide targeting Oct-1 transcription factor consensus sequence

Author(s): Xu Xiaoxin | Hong Xin | Wang Gan

A psychometric evaluation of the PedsQL™ Family Impact Module in parents of children with sickle cell disease

Author(s): Panepinto Julie | Hoffmann Raymond | Pajewski Nicholas

Primary stroke prevention for sickle cell disease in north-east Italy: the role of ethnic issues in establishing a Transcranial Doppler screening program

Author(s): Colombatti Raffaella | Meneghetti Giorgio | Ermani Mario | Pierobon Marta | Sainati Laura

Consanguinity and major genetic disorders in Saudi children : A community-based cross-sectional study

Author(s): El Mouzan Mohammad | Al Salloum Abdullah | Al Herbish Abdullah | Qurachi Mansour | Al Omar Ahmad

Asymptomatic malaria parasitaemia in sickle-cell disease patients: how effective is chemoprophylaxis ?

Author(s): Rachel Kotila | Abiola Okesola | Olufunmilola Makanjuola

Lupus anticoagulant and leg ulcers in sickle cell anemia

Author(s): Olayemi Edeghonghon | Bazuaye Godwin

Pattern of steroid resistant nephrotic syndrome in children living in the kingdom of Saudi Arabia: A single center study

Author(s): Kari Jameela | Halawani Manal | Mokhtar Ghadeer | Jalalah Sawsan | Anshasi Wasim

Sickle cell disease status among school adolescents and their tribal community in South Gujarat

Author(s): Bipin Vasava | Rajesh K Chudasama | Naresh R Godara | Ratan K Srivastava

Laparoscopic cholecystectomy in sickle cell patients in Niger

Author(s): Sani Rachid | Lassey James Didier | Mallam Abdou Badé | Chaibou Maman Sani | Abarchi Habibou

Inherited trombophilic states and pulmonary embolism

Author(s): Filip A. Konecny

Mutagenicity of New Lead Compounds to Treat Sickle Cell Disease Symptoms in a Salmonella/Microsome Assay

Author(s): Jean Leandro dos Santos | Eliana A. Varanda | Lídia Moreira Lima | Chung Man Chin

How to Reach Rapid Diagnosis in Sickle Cell Disease?

Author(s): Ehsan Valavi | Mohammad-Javad Alemzadeh Ansari | Khodamorad Zandian

The use of partial exchange blood transfusion and anaesthesia in the management of sickle cell disease in a perioperative setting: two case reports

Author(s): Jaeckel Rhett | Thieme Matthias | Czeslick Elke | Sablotzki Armin

High incidence of severe cyclosporine neurotoxicity in children affected by haemoglobinopaties undergoing myeloablative haematopoietic stem cell transplantation: early diagnosis and prompt intervention ameliorates neurological outcome

Spectrum of musculo-skeletal disorders in sickle cell disease in Lagos, Nigeria

Perturbation of the Developmental Potential of Preimplantation Mouse Embryos by Hydroxyurea

HEMATOPOIETIC STEM CELL TRNSPLANTATION IN THALASSEMIA AND RELATED DISORDERS

INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES

Author(s): Bianca Maria Ricerca | Arturo Di Girolamo | Deborah Rund

HEMATOPOIETIC STEM CELL TRANSPLANTATION IN THALASSEMIA AND SICKLE CELL DISEASE: EXPERIENCE OF MEDITERRANEAN INSTITUTE OF HEMATOLOGY IN A MULTI-ETHNIC POPULATION.

Author(s): Marco Marziali | Antonella Isgrò | Javid Gaziev | Guido Lucarelli

PATHOPHISIOLOGY OF SICKLE CELL DISEASE AND NEW DRUGS FOR THE TREATMENT

Author(s): Lucia De Franceschi

Treatment of steroid resistant nephrotic syndrome in children

Author(s): Kari Jameela | Halawani Manal

Tackling Africa's chronic disease burden: from the local to the global

Iron Overload in Sickle Cell Disease

Author(s): Radha Raghupathy | Deepa Manwani | Jane A. Little

Modifiable risk factors for ischemic stroke

Author(s): Alexandros Gianoulakis | Panagiota Konti

Acute chest syndrome in sickle cell disease in Saudi Arab Children in the Eastern Province.

Author(s): Al-Dabbous Ibrahim

Regional experience with newborn screening for sickle cell disease, other hemoglobinopathies and G6PD deficiency.

Salmonella as a causative organism of various infections in patients with sickle cell disease.

Author(s): Elbashier Ali | Al-Salem Ahmed | Aljama A

Observations on the management of acute pain crisis in adult sickle cell disease in eastern Saudi Arabia

Author(s): Udezue Emmanuel | Girshab Abdel

Zinc and antioxidant vitamin deficiency in patients with severe sickle cell anemia

Author(s): Hasanato Rana

An up-date on the prevalence of sickle cell trait in Eastern and Western Uganda

Depression and loneliness in Jamaicans with sickle cell disease

Author(s): Asnani Monika | Fraser Raphael | Lewis Norma | Reid Marvin

Public awareness of sickle cell disease in Bahrain

Author(s): Al Arrayed Shaikha | Al Hajeri Amani

Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya

Author(s): Marsh Vicki | Kamuya Dorcas | Mlamba Albert | Williams Thomas | Molyneux Sassy

Haematological Parameters of Sickle Cell Disease Patients with Menstruation Induced Vaso-Occlusive Crises

Author(s): S.G. Ahmed | J. Umana | U.A. Ibrahim

Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease in Burkina Faso

Evaluation of Antioxidant Levels and Trace Element Status in Nigerian Sickle Cell Disease Patients with Plasmodium Parasitaemia

Author(s): O.G. Arinola | J.A. Olaniyi | M.O. Akiibinu

Jaundice in typhoid patients: Differentiation from other common causes of fever and jaundice in the tropics

Author(s): Ahmed A | Ahmed B

Proteinuria in adult Saudi patients with sickle cell disease is not associated with identifiable risk factors

Author(s): Aleem Aamer

Sickle cell knowledge, premarital screening and marital decisions among local government workers in Ile-Ife, Nigeria

Author(s): Emmanuel A. Abioye-Kuteyi | Olanrewaju Oyegbade | Ibrahim Bello | Chiddude Osakwe

Intervention and Prevention of Hereditary Hemolytic Disorders in Two Ethnic Communities of Sundargarh District of Orissa, India: An Experience from KAP Studies

Author(s): Balgir RS

Modified port placement and pedicle first approach for laparoscopic concomitant cholecystectomy and splenectomy in children

Author(s): Pal Kamalesh

Refractory obstructive jaundice in a child affected with thalassodrepanocytosis: a new endoscopic approach

Double disadvantage: a case control study on health-related quality of life in children with sickle cell disease

Pathological basis of symptoms and crises in sickle cell disorder: implications for counseling and psychotherapy

Author(s): Oluwatoyin Olatundun Ilesanmi

Best practices for transfusion for patients with sickle cell disease

Author(s): Ted Wun | Kathryn Hassell

GENE MUTATIONS, GENETIC DISEASE AND PHARMACOGENETIC GENES DISORDER

Author(s): Ishak

Neuropsychological assessment, neuroimaging, and neuropsychiatric evaluation in pediatric and adult patients with sickle cell disease (SCD)

Angioid streaks, clinical course, complications, and current therapeutic management

Role of hydroxycarbamide in prevention of complications in patients with sickle cell disease

Author(s): NM Wiles | J Howard

Septic arthritis of the hips in adults with sickle cell anemia

Author(s): Alexandre Poignard | Mohamed Bouhou | Yasuhiro Homma | Philippe Hernigou

Proteinuria among adult sickle cell anemia patients in Nigeria

Author(s): Abdu A | Emokpae M | Uadia P | Kuliya-Gwarzo A

Anesthetic management of a patient with sickle β+ thalassemia

Author(s): Bharati Saswata | Das Subhabrata | Majee Prasenjit | Mandal Subrata

Author(s): Mostafa Abdel-Monhem Amr | Tarek Tawfik Amin | Omar Ahmed Al-Omair

Assessment of the In Vivo Genotoxicity of New Lead Compounds to Treat Sickle Cell Disease

Author(s): Jean Leandro dos Santos | Priscila Longhin Bosquesi | Eliana Aparecida Varanda | Lídia Moreira Lima | Man Chin Chung

Nitric oxide in gingival crevicular fluid and nitric oxide synthase expression in the gingiva of patients with sickle cell disease

Author(s): Esra Güzeldemir | Hilal Uslu Toygar | Nebil Bal | Ruksan Anarat | Can Boğa

THERAPEUTIC EFFICACY OF DADIM GHRITA IN THE MANAGEMENT OF SAHAJ PANDU ROGA (SICKLE CELL DISEASE): A HUMAN TRIAL BASED STUDY

Author(s): Shrivas Yogita Kameshwar | Shamkuwar Manoj Keshorao | Tiwari Gopinath | Shamkuwar Sujata Keshorao | Chauhan Amit Singh

Self-Care Recommendations of Middle-Aged and Older Adults with Sickle Cell Disease

Author(s): Coretta M. Jenerette | Cheryl Brewer | Ashley N. Leak

Pulmonary Spirometry Parameters in Patients with Sickle Thalassemia and Sickle Cell Disease at Shafa Hospital in Khuzestan Province-Iran

Author(s): Keikhaei B | Idani E | Samadi B | Titidage A

Raised D-dimer levels in acute sickle cell crisis and their correlation with chest X-ray abnormalities

Terminalia catappa Extract Enhances Erythropoiesis in Adult Balb C Mice

A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

Analysis of hepatitis C virus infection among sickle cell anemia patients by an antigen-antibody combination assay

Author(s): Obeid E. Obeid | Alhusain J. Alzahrani

How to Reach Rapid Diagnosis in Sickle Cell Disease?

Author(s): Ehsan Valavi | Mohammad-Javad Alemzadeh Ansari | Khodamorad Zandian

Mutagenic and Genotoxic Effect of Hydroxyurea

Author(s): Jean L. Santos | Priscila L. Bosquesi | Adélia E. Almeida | Chung Man Chin | Eliana A. Varand

Genetic Disease Burden, Nutrition and Determinants of Tribal Health Care in Chhattisgarh State of Central-East India: A Status Paper

Author(s): Balgir RS

Sickle Cell Disease and Pregnancy: Does Outcome Depend on Genotype or Phenotype?

Late fetal death after mid-trimestre elective myomectomy

Author(s): Ana Maria Coelho

Pathophysiological consequences of hemolysis. Role of cell-free hemoglobin

Author(s): Tomasz Misztal | Marian Tomasiak

Serum testosterone levels of HbSS (sickle cell disease) male subjects in Lagos, Nigeria

Knowledge of family health program practitioners in Brazil about sickle cell disease: a descriptive, cross-sectional study

Author(s): Gomes Ludmila | Vieira Magda | Reis Tatiana | Barbosa Thiago | Caldeira Antônio

Cause of death among Ghanaian adolescents in Accra using autopsy data

Author(s): Ohene Sally-Ann | Tettey Yao | Kumoji Robert

Best practices for transfusion for patients with sickle cell disease

Author(s): Ted Wun | Kathryn Hassell

Tricuspid regurgitant velocity elevation in a three-year old child with sickle cell anemia and recurrent acute chest syndromes reversed not by hydroxyurea but by bone marrow transplantation

Sickle cell protection from malaria: a review

Author(s): Sandro Eridani

Hydroxyurea Therapy Mobilises Arachidonic Acid from Inner Cell Membrane Aminophospholipids in Patients with Homozygous Sickle Cell Disease

Iron Overload Assessment in Adult Thalassaemic Patients Using MRI T2

Author(s): Azita Azarkeivan | Shahram Akhlaghpoor | Bashir Hajibeigi | Masoumeh Eslami | Afshan Shirkavand

Sickle cell hemoglobin D disease First reported case in IRAN

Author(s): mohamad mehdi aflatouni | mohamad malek

Homozygous hemoglobin D with alpha thalassemia: case report

Author(s): Sanjay Pandey | Rahasya Mani Mishra | Sweta Pandey | Renu Saxena

Anti Sickle Erythrocytes Haemolysis Properties and Inhibitory Effect of Anthocyanins Extracts of Trema orientalis (Ulmaceae) on the Aggregation of Human Deoxyhemoglobin S in vitro

Epidemiology of sickle cell disease in Saudi Arabia

Author(s): Jastaniah Wasil

Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia

Author(s): Memish Ziad | Saeedi Mohammad

Acute abdominal conditions in people with sickle cell disease: A 10-year experience in Port Harcourt, Nigeria

Author(s): Jebbin N | Adotey J

Iron Depletion: An Ameliorating Factor for Sickle Cell Disease?

Author(s): P. C. Giordano | W. Huisman | C. L. Harteveld

Sickle cell hemoglobinopathy protection against malaria: is it changing?

Author(s): Arti Prasad Muley | Jitendra Lakhani, Maulik Parikh

Pulmonary function in adults with sickle cell disease

Author(s): Sandip Meghnad Hulke | Avinash Eknath Thakare

SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM

Author(s): Zohreh Rahimi | Abbas Parsian

THE ROLE OF INFECTION IN THE PATHOGENESIS OF VASO-OCCLUSIVE CRISIS IN PATIENTS WITH SICKLE CELL DISEASE.

Author(s): SAGIR GUMEL AHMED

Community Acquired Bacteremia in Young Children from Central Nigeria- A Pilot Study

Determination of serum C and S protein and factor V leiden in sickle cell disorder in Khozestan province

Author(s): Pedram Mohammad | Keikhai Bijan | Fathi Afshin

Response to Radiation in Renal Medullary Carcinoma: a Case Report and Review of the Literature

Author(s): Alexandra M. Walsh | John B. Fiveash | Alyssa T. Reddy | Gregory K. Friedman

Antiradical, Chelating and Antioxidant Activities of Hydroxamic Acids and Hydroxyureas

Author(s): Marijana Zovko Končić | Monika Barbarić | Ivana Perković | Branka Zorc

Indigenous Traditional Medical Practitioners’ Lack of Formal Medical Education Impacts their Choices of Information Resources for the Treatment of Sickle Cell Anemia. A Review of: Olatokun, W. M., & Ajagbe, E. (2010). Analyzing traditional medical practitioners’ information-seeking behavior using Taylor’s information-use environment model. Journal of Librarianship and Information Science, 42, 122-135.

Author(s): Maria C. Melssen

Pattern of AST and ALT Changes in Relation to Hemolysis in Sickle Cell Disease

Incidence of alloimunization in sickle cell disease: experience of a center in São Paulo

Author(s): Ricardo Helman | Rodolfo Delfini Cançado | Cristina Olivatto

Comparative evolutionary analyses of beta globin gene in eutherian, dinosaurian and neopterygii taxa

Author(s): Gauri Awasthi, Garima Srivastava & Aparup Das

Moringa oleifera Lamarck (drumstick) Leaf Extract Modulates the Evidences of Hydroxyurea -Induced Testicular Derangement

A Case of Refractory Salmonella Spondylodiscitis in an Immunocompetent Patient Treated Via an Extracavitary Approach, Corpectomy and Placement of Expandable Cage

Author(s): Kimon Bekelis | Oren Gottfried | Zyia L. Gokaslan | Panagiotis Markopoulos | Ibrahim Omeis

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