Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Fetal anemia; Nonimmune hydrops fetalis; Autosomal recessive; α-Spectrin; SPTA1;
مقالات ISI اسپرهسیتوز ارثی (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: اسپرهسیتوز ارثی; HS; hereditary spherocytosis; LF; lymphoid follicle; MZ; marginal zone; RBC; red blood cell; SCD; sickle-cell disease; SMA; smooth muscle actin.; Hereditary spherocytosis; Sickle cell disease; Spleen; Vasculopathy; Splenic pathophysiology;
Keywords: اسپرهسیتوز ارثی; RBC; red blood cell; NGS; next-generation sequencing; HS; hereditary spherocytosis; SNV; single nucleotide variants; HE; hereditary elliptocytosis; ANK1; ankyrin 1; SPTB; spectrin, beta, erythrocytic; SPTA1; spectrin alpha, erythrocytic 1; SLC4A1; solute
Keywords: اسپرهسیتوز ارثی; AIHA; auto-immune hemolytic anemia; CBC; complete blood count; CDA; congenital dyserythropoietic anemia; CHCM; Cell Hemoglobin Concentration Mean; CV; coefficient of variation; DAT; direct agglutination test; DHSt; dehydrated hereditary stomatocytosis (xe
Keywords: اسپرهسیتوز ارثی; anaemia; cholelithiasis; haemolysis; hereditary spherocytosis; jaundice; splenomegaly
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Glucose-6-phosphate dehydrogenase deficiency; Gilbert syndrome; Alpha gene deletion
Extramedullary hematopoiesis of the sphenoid sinus associated with hereditary spherocytosis: A case report
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Extramedullary hematopoiesis; Sinonasal mass; Paranasal sinuses;
Inherited anaemias: sickle cell and thalassaemia
Keywords: اسپرهسیتوز ارثی; G6PD deficiency; hereditary spherocytosis; inherited haemolytic anaemia; sickle cell disease; thalassaemia;
Extramedullary Hematopoiesis Mimicking Mediastinal Tumor in a Patient with Hereditary Spherocytosis: Case report
Keywords: اسپرهسیتوز ارثی; Hematopoiesis, extramedullay; Mediastinal mass or neoplasm; Hereditary spherocytosis; Video assisted thoracoscopic surgery (VATS); A case report;
CASE 5-2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell Fragility
Keywords: اسپرهسیتوز ارثی; hereditary spherocytosis; extracorporeal circulation; cardiopulmonary bypass; red blood cell fragility; hemolysis; congenital cardiac surgery;
Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Mean sphered corpuscular volume; Misdiagnosis
Crisis aplásica por Parvovirus B19 y virus de Epstein-Barr en paciente con esferocitosis hereditaria
Keywords: اسپرهسیتوز ارثی; Anemia hemolítica; Crisis aplásica; Esferocitosis hereditaria; Virus de Epstein-Barr; Parvovirus B19Hemolytic anemia; Aplastic crisis; Hereditary spherocytosis; Epstein-Barr virus; Parvovirus B19
Révélation à l'âge adulte d'une sphérocytose héréditaire devant une tumeur rénale : forme frontière entre myélolipome et foyer d'hématopoïèse extra-médullaire
Keywords: اسپرهسیتوز ارثی; Hématopoïèse extra-médullaire; Myélolipome; Imagerie nucléaire; Tumeurs rénales; Sphérocytose héréditaire atypique; Extramedullary hematopoiesis; Myelolipoma; Radionuclide imaging; Kidney neoplasms; Hereditary spherocytosis;
Inherited anaemias: sickle cell and thalassaemia
Keywords: اسپرهسیتوز ارثی; G6PD deficiency; hereditary spherocytosis; inherited haemolytic anaemia; sickle cell disease; thalassaemia
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Elliptocytosis; Pyropoikilocytosis; Stomatocytosis; Red cell membrane; Hemolysis
Abnormalities of the Erythrocyte Membrane
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Hereditary elliptocytosis; Hereditary pyropoikilocytosis; Erythrocyte membrane; Anemia; Splenectomy;
A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features
Keywords: اسپرهسیتوز ارثی; FGFR1; fibroblast growth factor receptor 1 gene; ANK1; ankyrin 1 gene; OFC; occipitofrontal circumference; SD; standard deviation; MCV; mean corpuscular volume; MCH; mean corpuscular hemoglobin; MCHC; mean corpuscular hemoglobin concentration; LH; luteini
Comparative Effectiveness of Different Types of Splenectomy for Children with Congenital Hemolytic Anemias
Keywords: اسپرهسیتوز ارثی; ACS; Acute chest syndrome; CHA; Congenital hemolytic anemias; DA; Dyserythropoietic anemia; Hgb; Hemoglobin; HJB; Howell-Jolly bodies; HS; Hereditary spherocytosis; MeSH; Medical subject headings; RBC; Red blood cell; SCD; Sickle cell disease;
Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Clinical outcome; Severity markers
Partial splenectomy for hereditary spherocytosis: a multi-institutional review
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Partial splenectomy; Multi-institutional review; Outcomes data
Institutional experience with laparoscopic partial splenectomy for hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Partial splenectomy; Partial laparoscopic splenectomy; Pediatric
Hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Red cell membrane; Hemolytic anemia; Diagnosis; TherapySphérocytose héréditaire; Membrane érythrocytaire; Anémie hémolytique; Diagnostic; Thérapie
Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model
Keywords: اسپرهسیتوز ارثی; Hereditary Spherocytosis; Anemia; KLF1; EKLF; Mouse mutant
PrzydatnoÅÄ cytometrycznej analizy biaÅek cytoszkieletu i bÅon erytrocytów (test EMA) w diagnozowaniu wrodzonych niedokrwistoÅci hemolitycznych u dzieci
Keywords: اسپرهسیتوز ارثی; sferocytoza wrodzona; cytometria przepÅywowa; bÅona i cytoszkielet krwinki czerwonej; hereditary spherocytosis; flow cytometry; erythrocyte membrane and cytoskeleton;
Inherited haemolytic anaemias
Keywords: اسپرهسیتوز ارثی; glucose-6-phosphate dehydrogenase deficiency; haemoglobinopathy; haemolytic anaemia; hereditary spherocytosis; sickle cell disease; thalassaemia
Hematologic characterization and chromosomal localization of the novel dominantly inherited mouse hemolytic anemia, neonatal anemia (Nan)
Keywords: اسپرهسیتوز ارثی; Hemolytic anemia; Mouse model; Hereditary spherocytosis; Bone marrow transplantation; Erythrocyte membrane skeleton
Compound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; anion exchanger 1; distal renal tubular acidosis; hereditary spherocytosis
Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Hemoglobinopathy; Laparoscopic splenectomy; Laparoscopic subtotal splenectomy; Postsplenectomy sepsis; Postoperative management
Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Peroxiredoxin 2; Oxidative stress; Erythrocyte membrane proteins; Mass-spectroscopy;
Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations
Keywords: اسپرهسیتوز ارثی; Hereditary spherocytosis; Hemoglobin oxidation; Carbonylation; Opsonization; Lipid rafts
Characterization of red cell membrane proteins as a function of red cell density:: Annexin VII in different forms of hereditary spherocytosis
Keywords: اسپرهسیتوز ارثی; Red blood cell; Membrane proteins; Proteomics; Hereditary spherocytosis; Annexin VII; Mass spectrometry2DE, two-dimensional electrophoresis; HS, hereditary spherocytosis; LCMS/MS, liquid chromatography coupled to tandem mass spectrometry; MALDI-TOF, matri
Disorders of the red cell membrane
Keywords: اسپرهسیتوز ارثی; Red cell; Membrane defects; Hereditary spherocytosis; Haemolytic anaemia; Children;
Prosthetic heart valves' mechanical loading of red blood cells in patients with hereditary membrane defects
Keywords: اسپرهسیتوز ارثی; Hemolysis; Valve (disease); Blood flow; Erythrocyte; Hereditary spherocytosis; Hereditary elliptocytosis; Prosthetic heart valves;