X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (46) 46
life sciences & biomedicine (45) 45
humans (44) 44
female (28) 28
male (25) 25
child (23) 23
hematology (20) 20
adolescent (19) 19
child, preschool (16) 16
adult (15) 15
middle aged (10) 10
oncology (10) 10
polycythemia (10) 10
mutation (9) 9
pediatrics (9) 9
congenital erythrocytosis (8) 8
genetic aspects (8) 8
genetics & heredity (8) 8
infant (8) 8
polycythemia - genetics (8) 8
children (7) 7
patients (7) 7
pedigree (7) 7
analysis (6) 6
genetic disorders (6) 6
polycythemia vera (6) 6
thalassemia (6) 6
young adult (6) 6
aged (5) 5
cancer (5) 5
erythrocytosis (5) 5
genetics (5) 5
infant, newborn (5) 5
polycythemia - diagnosis (5) 5
research (5) 5
treatment outcome (5) 5
adolescents (4) 4
age (4) 4
beta-thalassemia - complications (4) 4
diagnosis (4) 4
dna mutational analysis (4) 4
fertility (4) 4
genetic predisposition to disease (4) 4
genotype (4) 4
health aspects (4) 4
janus kinase 2 - genetics (4) 4
medical and health sciences (4) 4
medicin och hälsovetenskap (4) 4
polycythemia - congenital (4) 4
polycythemia vera - genetics (4) 4
polymorphism, single nucleotide (4) 4
abridged index medicus (3) 3
adolescence (3) 3
base sequence (3) 3
beta-thalassemia - blood (3) 3
bone marrow - pathology (3) 3
cancer therapies (3) 3
childhood (3) 3
chromosome 19q13 (3) 3
development and progression (3) 3
erythropoiesis (3) 3
genetic variation (3) 3
germany (3) 3
girls (3) 3
glucose tolerance test (3) 3
guidelines (3) 3
internal medicine (3) 3
iron overload (3) 3
late effects (3) 3
magnetic resonance imaging (3) 3
medicine (3) 3
medicine & public health (3) 3
methods (3) 3
ototoxicity (3) 3
physiological aspects (3) 3
polycythemia vera - diagnosis (3) 3
polymerase chain reaction (3) 3
precursor cell lymphoblastic leukemia-lymphoma - genetics (3) 3
prognosis (3) 3
prospective studies (3) 3
quality of life (3) 3
receptors, erythropoietin - genetics (3) 3
research article (3) 3
retrospective studies (3) 3
sensitivity and specificity (3) 3
sickle cell disease (3) 3
signal transduction - genetics (3) 3
stem cells (3) 3
abnormalities (2) 2
aged, 80 and over (2) 2
algorithms (2) 2
animals (2) 2
benzoates - therapeutic use (2) 2
beta-thalassemia - drug therapy (2) 2
birth (2) 2
bone marrow transplantation (2) 2
budd-chiari syndrome (2) 2
cancer and oncology (2) 2
cancer och onkologi (2) 2
cancer survivors (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


DMW - Deutsche Medizinische Wochenschrift, ISSN 0012-0472, 06/2019, Volume 144, Issue 11, pp. 719 - 723
Was ist neu? Therapie der Thalassämien  1. Schwere α-Thalassämie: Der intrauterine Beginn einer postnatal fortgeführten Transfusionstherapie (Alternative:... 
Klinischer Fortschritt
Journal Article
by Taylor, Jenny C and Martin, Hilary C and Lise, Stefano and Broxholme, John and Cazier, Jean-Baptiste and Rimmer, Andy and Kanapin, Alexander and Lunter, Gerton and Fiddy, Simon and Allan, Chris and Aricescu, A Radu and Attar, Moustafa and Babbs, Christian and Becq, Jennifer and Beeson, David and Bento, Celeste and Bignell, Patricia and Blair, Edward and Buckle, Veronica J and Bull, Katherine and Cais, Ondrej and Cario, Holger and Chapel, Helen and Copley, Richard R and Cornall, Richard and Craft, Jude and Dahan, Karin and Davenport, Emma E and Dendrou, Calliope and Devuyst, Olivier and Fenwick, Aimée L and Flint, Jonathan and Fugger, Lars and Gilbert, Rodney D and Goriely, Anne and Green, Angie and Greger, Ingo H and Grocock, Russell and Gruszczyk, Anja V and Hastings, Robert and Hatton, Edouard and Higgs, Doug and Hill, Adrian and Holmes, Chris and Howard, Malcolm and Hughes, Linda and Humburg, Peter and Johnson, David and Karpe, Fredrik and Kingsbury, Zoya and Kini, Usha and Knight, Julian C and Krohn, Jonathan and Lamble, Sarah and Langman, Craig and Lonie, Lorne and Luck, Joshua and McCarthy, Davis and McGowan, Simon J and McMullin, Mary Frances and Miller, Kerry A and Murray, Lisa and Németh, Andrea H and Nesbit, M Andrew and Nutt, David and Ormondroyd, Elizabeth and Oturai, Annette Bang and Pagnamenta, Alistair and Patel, Smita Y and Percy, Melanie and Petousi, Nayia and Piazza, Paolo and Piret, Sian E and Polanco-Echeverry, Guadalupe and Popitsch, Niko and Powrie, Fiona and Pugh, Chris and Quek, Lynn and Robbins, Peter A and Robson, Kathryn and Russo, Alexandra and Sahgal, Natasha and van Schouwenburg, Pauline A and Schuh, Anna and Silverman, Earl and Simmons, Alison and Sørensen, Per Soelberg and Sweeney, Elizabeth and Taylor, John and Thakker, Rajesh V and Tomlinson, Ian and Trebes, Amy and Twigg, Stephen R F and Uhlig, Holm H and Vyas, Paresh and Vyse, Tim and Wall, Steven A and Watkins, Hugh and Whyte, Michael P and Witty, Lorna and ...
Nature genetics, ISSN 1061-4036, 05/2015, Volume 47, Issue 7, pp. 717 - 726
Journal Article
Deutsches Ärzteblatt international, ISSN 1866-0452, 03/2012, Volume 109, Issue 10, pp. 190 - 190
Journal Article
Haematologica (Roma), ISSN 0390-6078, 10/2016, Volume 101, Issue 11, pp. 1306 - 1318
Erythrocytosis is a rare disorder characterized by increased red cell mass and elevated hemoglobin concentration and hematocrit. Several genetic variants have... 
Life Sciences & Biomedicine | Hematology | Science & Technology | Genetic Variation | Polycythemia - diagnosis | Polycythemia - genetics | Molecular Diagnostic Techniques - methods | Polycythemia - etiology | Humans | Molecular Diagnostic Techniques - standards | Mutation | Sequence Analysis, DNA | Index Medicus
Journal Article
Journal Article
American journal of hematology, ISSN 0361-8609, 02/2016, Volume 91, Issue 2, pp. 248 - 251
Journal Article
Memo - Magazine of European medical oncology, ISSN 1865-5076, 04/2018, Volume 11, Issue 3, pp. 235 - 240
... Holger Cario Received: 19 February 2018 / Accepted: 27 March 2018 / Published online: 13 April 2018 © Springer-Verlag GmbH Austria, part of Springer Nature 2018... 
Iron overload | Hemoglobinopathy | Medicine & Public Health | Alpha-thalassemia | Oncology | Beta-thalassemia | Sickle cell disease | Medicine/Public Health, general | Development and progression | Sickle cell anemia
Journal Article
British journal of haematology, ISSN 0007-1048, 05/2014, Volume 165, Issue 4, pp. 519 - 528
Summary Primary familial and congenital polycythaemia (PFCP) is a disease characterized by increased red blood cell mass, and can be associated with mutations... 
myeloproliferative disorder