Found: 56
Select item for more details and to access through your institution.
Nonimmune Hydrops Fetalis due to Congenital Xerocytosis.
- Published in:
- 2005
- By:
- Publication type:
- Abstract
Cutaneous Myeloid Metaplasia with Dysplastic Features in Idiopathic Myelofibrosis.
- Published in:
- International Journal of Dermatology, 1988, v. 27, n. 3, p. 179, doi. 10.1111/j.1365-4362.1988.tb04926.x
- By:
- Publication type:
- Article
Distinguishing iron deficiency from beta‐thalassemia trait by new generation ektacytometry.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor
Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose‐6‐phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
Effect of EDTA-anticoagulated whole blood storage on cell morphology examination. A need for standardization.
- Published in:
- International Journal of Laboratory Hematology, 2014, v. 36, n. 2, p. 222, doi. 10.1111/ijlh.12170
- By:
- Publication type:
- Article
Haemoglobinopathies in Europe: health & migration policy perspectives.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-97
- By:
- Publication type:
- Article
Haemoglobinopathies in Europe: health & migration policy perspectives.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Insights into the Role of Bioactive Food Ingredients and the Microbiome in Idiopathic Pulmonary Fibrosis.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 17, p. 6051, doi. 10.3390/ijms21176051
- By:
- Publication type:
- Article
The value of organ and tissue biovigilance: a cross-sectional analysis.
- Published in:
- Frontiers in Transplantation, 2024, p. 1, doi. 10.3389/frtra.2024.1307946
- By:
- Publication type:
- Article
SARS‐CoV‐2 detection in bioaerosols using a liquid impinger collector and ddPCR.
- Published in:
- Indoor Air, 2022, v. 32, n. 2, p. 1, doi. 10.1111/ina.13002
- By:
- Publication type:
- Article
Criteria for assigning laboratory measurands to models for analytical performance specifications defined in the 1st EFLM Strategic Conference.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 2, p. 189, doi. 10.1515/cclm-2016-0091
- By:
- Publication type:
- Article
Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Understanding Rare Anemias: Emerging Frontiers for Diagnosis and Treatment.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 11, p. 3180, doi. 10.3390/jcm13113180
- By:
- Publication type:
- Article
Crystal structure of a helical oligopeptide model of polyglycine II and of other polyamides: Acetyl-(glycyl-β-alanyl)<sub>2</sub>- NH propyl.
- Published in:
- Biopolymers, 1992, v. 32, n. 6, p. 643, doi. 10.1002/bip.360320607
- By:
- Publication type:
- Article
SARS-CoV-2 Infection and Anemia—A Focus on RBC Deformability and Membrane Proteomics—Integrated Observational Prospective Study.
- Published in:
- Microorganisms, 2024, v. 12, n. 3, p. 453, doi. 10.3390/microorganisms12030453
- By:
- Publication type:
- Article
Red Cell Properties after Different Modes of Blood Transportation.
- Published in:
- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2016.00288
- By:
- Publication type:
- Article
First description of phosphofructokinase deficiency in spain: identification of a novel homozygous missense mutation in the PFKM gene.
- Published in:
- Frontiers in Physiology, 2013, v. 4, p. 1, doi. 10.3389/fphys.2013.00393
- By:
- Publication type:
- Article
Combined assay of adenosine deaminase, purine nucleoside phosphorylase, and lactate dehydrogenase in the early clinical evaluation of B-chronic lymphocytic leukemia.
- Published in:
- American Journal of Hematology, 1988, v. 27, n. 3, p. 157, doi. 10.1002/ajh.2830270302
- By:
- Publication type:
- Article
Recommendations for centres of expertise in rare anaemias. The ENERCA White Book.
- Published in:
- Thalassemia Reports, 2014, v. 4, n. 3, p. 86, doi. 10.4081/thal.2014.4878
- By:
- Publication type:
- Article
ENERCA - European Network for Rae and Congenital Anaemias 2002-2012. 10 years of life.
- Published in:
- Thalassemia Reports, 2013, v. 3, n. 1s, p. 109, doi. 10.4081/thal.2013.s1.e44
- By:
- Publication type:
- Article
Y-body study in bone marrow precursors, peripheral blood cells and alveolar macrophages for demonstration of haemopoietic engraftment in allogeneic bone marrow transplantation.
- Published in:
- European Journal of Haematology, 1988, v. 40, n. 5, p. 424, doi. 10.1111/j.1600-0609.1988.tb00851.x
- By:
- Publication type:
- Article
European expert network on rare communicable diseases and other rare diseases linked to mobility and globalisation focused on health care provision (EURaDMoG): a feasibility study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Rectus abdominis muscle injuries in elite handball players: management and reha.
- Published in:
- Open Access Journal of Sports Medicine, 2011, v. 2, p. 69, doi. 10.2147/OAJSM.S17504
- By:
- Publication type:
- Article
B-Type Large-Cell Primary Splenic Lymphoma with Massive Involvement of the Red Pulp.
- Published in:
- Acta Haematologica, 1993, v. 89, n. 1, p. 46, doi. 10.1159/000204483
- By:
- Publication type:
- Article
Acquired Amegakaryocytic Thrombocytopenic Purpura Associated with Immunoglobulin Deficiency.
- Published in:
- Acta Haematologica, 1991, v. 85, n. 1, p. 34, doi. 10.1159/000204849
- By:
- Publication type:
- Article
Chronic Neutrophilic Leukemia with Dysplastic Features.
- Published in:
- Acta Haematologica, 1990, v. 84, n. 2, p. 109, doi. 10.1159/000205042
- By:
- Publication type:
- Article
Chronic Myelomonocytic Leukemia Associated with Hereditary Pyruvate Kinase Deficiency and Multiple Acquired Erythrocyte Abnormalities.
- Published in:
- Acta Haematologica, 1979, v. 61, n. 3, p. 168, doi. 10.1159/000207651
- By:
- Publication type:
- Article
Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry.
- Published in:
- International Journal of Hematology, 2021, v. 113, n. 2, p. 163, doi. 10.1007/s12185-020-03010-9
- By:
- Publication type:
- Article
Oxidative stress and other risk factors for white matter lesions in chronic hemodialysis patients.
- Published in:
- Clinical Nephrology, 2013, v. 80, n. 3, p. 187, doi. 10.5414/CN107943
- By:
- Publication type:
- Article
Low affinity hemoglobinopathy ( Hb Vigo) due to a new mutation of beta globin gene (c200 A> T; Lys> Ile). A cause of rare anemia misdiagnosis.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 4, p. E38, doi. 10.1002/ajh.24649
- By:
- Publication type:
- Article
Uso de la práctica imaginada para el afrontamiento de la competición en piragüismo slalom.
- Published in:
- Revista de Psicología Aplicada al Deporte & al Ejercicio Físico, 2022, v. 7, n. 2, p. 1, doi. 10.5093/rpadef2022a13
- By:
- Publication type:
- Article
Integración de rutinas competitivas como hábito de entrenamiento en jugadores de tenis de mesa.
- Published in:
- Revista de Psicología Aplicada al Deporte & al Ejercicio Físico, 2022, v. 7, n. 2, p. 1, doi. 10.5093/rpadef2022a11
- By:
- Publication type:
- Article
In Vivo and In Vitro Pro-Fibrotic Response of Lung-Resident Mesenchymal Stem Cells from Patients with Idiopathic Pulmonary Fibrosis.
- Published in:
- Cells (2073-4409), 2024, v. 13, n. 2, p. 160, doi. 10.3390/cells13020160
- By:
- Publication type:
- Article
Mitochondrial Dysfunction in Lung Resident Mesenchymal Stem Cells from Idiopathic Pulmonary Fibrosis Patients.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 16, p. 2084, doi. 10.3390/cells12162084
- By:
- Publication type:
- Article
Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias.
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00386
- By:
- Publication type:
- Article
Two new phosphoglycerate kinase mutations associated with chronic haemolytic anaemia and neurological dysfunction in two patients from Spain.
- Published in:
- British Journal of Haematology, 2006, v. 132, n. 4, p. 523, doi. 10.1111/j.1365-2141.2005.05882.x
- By:
- Publication type:
- Article
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies.
- Published in:
- British Journal of Haematology, 2001, v. 112, n. 2, p. 475, doi. 10.1046/j.1365-2141.2001.02526.x
- By:
- Publication type:
- Article
Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1159, doi. 10.1002/humu.9466
- By:
- Publication type:
- Article
mTOR inhibition and erythropoiesis: microcytosis or anaemia?
- Published in:
- Nephrology Dialysis Transplantation, 2012, v. 27, n. 2, p. 537, doi. 10.1093/ndt/gfr318
- By:
- Publication type:
- Article
The development and implementation of an oxygen treatment solution for health facilities in low and middle-income countries.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Blood Rheological Characterization of β-Thalassemia Trait and Iron Deficiency Anemia Using Front Microrheometry.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.761411
- By:
- Publication type:
- Article
Tension gastrothorax mimicking acute coronary syndrome and causing cardiac arrest.
- Published in:
- European Heart Journal, 2014, v. 35, n. 12, p. 794, doi. 10.1093/eurheartj/eht336
- By:
- Publication type:
- Article
Investigadores académicos y profesionales de la Psicología del Deporte: Condenados a entenderse.
- Published in:
- Journal of Sport Psychology / Revista de Psicología del Deporte, 2017, v. 26, p. 80
- By:
- Publication type:
- Article
Psicología aplicada al Balonmano.
- Published in:
- 2008
- By:
- Publication type:
- Book Review
α-thalassaemia due to a single codon deletion in the α-1-globin gene. Computational structural analysis of the new α-chain variant.
- Published in:
- Human Mutation, 1998, v. 11, n. 5, p. 412, doi. 10.1002/(SICI)1098-1004(1998)11:5<412::AID-HUMU14>3.0.CO;2-R
- By:
- Publication type:
- Article
Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase gene.
- Published in:
- Human Mutation, 1996, v. 8, n. 4, p. 311, doi. 10.1002/(SICI)1098-1004(1996)8:4<311::AID-HUMU3>3.0.CO;2-A
- By:
- Publication type:
- Article
The glucose-6-phosphate dehydrogenase (G6PD) deficient variant G6PD union (454 Arg→Cys) has a worldwide distribution possibly due to recurrent mutation.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 5, p. 833
- By:
- Publication type:
- Article
Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?
- Published in:
- Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00673
- By:
- Publication type:
- Article
FIRST DESCRIPTION OF A FRAMESHIFT MUTATION IN THE α<sub>1</sub>-GLOBIN GENE ASSOCIATED WITH α-THALASSAEMIA.
- Published in:
- British Journal of Haematology, 1997, v. 98, n. 1, p. 47, doi. 10.1046/j.1365-2141.1997.1822999.x
- By:
- Publication type:
- Article
Bone marrow assessment in B-cell chronic lymphocytic leukaemia: aspirate or biopsy? A comparative study in 258 patients.
- Published in:
- British Journal of Haematology, 1996, v. 93, n. 1, p. 111, doi. 10.1046/j.1365-2141.1996.449988.x
- By:
- Publication type:
- Article