X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (18) 18
humans (15) 15
hematology (12) 12
female (11) 11
child (9) 9
male (9) 9
child, preschool (8) 8
adult (7) 7
mutation (6) 6
adolescent (5) 5
middle aged (5) 5
phenotype (5) 5
young adult (5) 5
diagnosis (4) 4
disorders (4) 4
fanconi's anemia (4) 4
genetic aspects (4) 4
genotype (4) 4
mutation, missense (4) 4
mutations (4) 4
pedigree (4) 4
platelet count (4) 4
thrombocytopenia (4) 4
thrombocytopenia - genetics (4) 4
ciencias médicas y de la salud (3) 3
complementation group-a (3) 3
complex i defects (3) 3
families (3) 3
fanconi anemia - genetics (3) 3
gene (3) 3
genetic association studies (3) 3
genetics & heredity (3) 3
hemic and lymphatic diseases (3) 3
heterozygote (3) 3
italy (3) 3
macrothrombocytopenia (3) 3
medicina clínica (3) 3
original (3) 3
thrombocytopenia - diagnosis (3) 3
thrombopoietin - blood (3) 3
aged (2) 2
aged, 80 and over (2) 2
alleles (2) 2
amino acid sequence (2) 2
amino acid substitution (2) 2
anemia (2) 2
article (2) 2
articles (2) 2
bernard-soulier syndrome (2) 2
bernard-soulier syndrome - genetics (2) 2
bernard-soulier-syndrome (2) 2
blood platelets - metabolism (2) 2
blood platelets - pathology (2) 2
blood platelets - ultrastructure (2) 2
blood proteins - genetics (2) 2
bone marrow (2) 2
cancer (2) 2
cells (2) 2
defects (2) 2
dna repair - genetics (2) 2
energy metabolism (2) 2
exons (2) 2
gene expression (2) 2
genes (2) 2
genes, dominant (2) 2
glycolysis (2) 2
glycoprotein-ib-alpha (2) 2
gray platelet syndrome - genetics (2) 2
health aspects (2) 2
hematología (2) 2
hemorrhage (2) 2
inherited thrombocytopenia (2) 2
inherited thrombocytopenias (2) 2
leucine-rich repeat (2) 2
management (2) 2
membrane glycoproteins - genetics (2) 2
metabolism (2) 2
mitochondria (2) 2
molecular sequence data (2) 2
mosaicism (2) 2
multidisciplinary sciences (2) 2
oxidative phosphorylation (2) 2
oxidative stress (2) 2
oxidative-phosphorylation (2) 2
patients (2) 2
physiological aspects (2) 2
platelet aggregation (2) 2
platelet-function (2) 2
point mutation (2) 2
polymorphism (2) 2
polymorphism, single nucleotide (2) 2
repair (2) 2
settore med/09 - medicina interna (2) 2
tropical medicine (2) 2
101 (1) 1
abnormalities (1) 1
abridged index medicus (1) 1
accumulation (1) 1
actinin (1) 1
actinin - genetics (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


British Journal of Haematology, ISSN 0007-1048, 10/2018, Volume 183, Issue 2, pp. 276 - 288
The inherited thrombocytopenias ( IT ) are a heterogeneous group of diseases resulting from mutations in more than 30 different genes. Among them, ACTN 1... 
ACTN | mutations | gene | thrombocytopenia | related thrombocytopenia | macrocytosis | ACTN1 gene | ACTN1-related thrombocytopenia | DOMAIN | INHERITED THROMBOCYTOPENIAS | CONGENITAL MACROTHROMBOCYTOPENIA | FAMILIES | DISORDERS | HEMATOLOGY | Thrombocytopenia | Genetic aspects | Clinical aspects | Actinin | Benign | Isoforms | Muscles | Heredity | Mutation | Platelets | Bleeding | Index Medicus
Journal Article
Haematologica, ISSN 0390-6078, 01/2012, Volume 97, Issue 1, pp. 82 - 88
Journal Article
Haematologica, ISSN 0390-6078, 03/2011, Volume 96, Issue 3, pp. 417 - 423
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 06/2017, Volume 1863, Issue 6, pp. 1214 - 1221
Journal Article
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 03/2015, Volume 230, Issue 3, pp. 603 - 609
Journal Article
American Journal of Hematology, ISSN 0361-8609, 02/2017, Volume 92, Issue 2, pp. E20 - E22
Journal Article
American Journal of Hematology, ISSN 0361-8609, 06/2017, Volume 92, Issue 6, pp. E86 - E88
Journal Article
Birth Defects Research Part A: Clinical and Molecular Teratology, ISSN 1542-0752, 12/2015, Volume 103, Issue 12, pp. 1003 - 1010
Journal Article
Journal Article