X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (16) 16
female (11) 11
index medicus (11) 11
male (9) 9
thailand (9) 9
adult (8) 8
mutation (7) 7
genetics & heredity (5) 5
hematology (5) 5
analysis (4) 4
case report (4) 4
genes (4) 4
genetic aspects (4) 4
hemoglobin (4) 4
hemoglobins, abnormal - genetics (4) 4
middle aged (4) 4
phenotype (4) 4
thalassemia (4) 4
alpha-thalassemia (3) 3
asian continental ancestry group - genetics (3) 3
diagnosis (3) 3
genetic association studies (3) 3
genetic research (3) 3
genetic screening (3) 3
genetics (3) 3
genotype (3) 3
in vitro fertilization (3) 3
medical research (3) 3
medicine & public health (3) 3
medicine, experimental (3) 3
next-generation sequencing (3) 3
pank2 (3) 3
alpha-thalassemia - diagnosis (2) 2
alpha-thalassemia - genetics (2) 2
anemia (2) 2
aneuploidy (2) 2
article subject (2) 2
asian continental ancestry group (2) 2
asians (2) 2
case-control studies (2) 2
children (2) 2
comparative genomic hybridization (2) 2
disease (2) 2
diseases of the endocrine glands. clinical endocrinology (2) 2
embryo transfer (2) 2
embryos (2) 2
family (2) 2
gene mutations (2) 2
gene sequencing (2) 2
genetic polymorphisms (2) 2
genetic predisposition to disease (2) 2
genomics (2) 2
globins - genetics (2) 2
gynecology (2) 2
hallervorden-spatz-syndrome (2) 2
health aspects (2) 2
hemoglobinopathy (2) 2
hospitals (2) 2
linkage analysis (2) 2
logistic models (2) 2
medicine (2) 2
methods (2) 2
molecular characterization (2) 2
oncology (2) 2
oral (2) 2
osteoarthritis, knee - genetics (2) 2
part 4 (2) 2
part 4: oral/poster (2) 2
pathogenesis (2) 2
patient (2) 2
polymerase chain reaction - methods (2) 2
poster (2) 2
pregnancy (2) 2
preimplantation genetic diagnosis (2) 2
prevalence (2) 2
pulse oximetry (2) 2
research (2) 2
risk factors (2) 2
sequence deletion (2) 2
asp (1) 1
abnormalities (1) 1
ace (1) 1
ace inhibitors (1) 1
acid repeat polymorphism (1) 1
adenocarcinoma - complications (1) 1
adenocarcinoma - physiopathology (1) 1
adenocarcinoma - surgery (1) 1
adipocyte differentiation (1) 1
adrenal adenoma (1) 1
adrenal glands (1) 1
aged (1) 1
aged, 80 and over (1) 1
alleles (1) 1
alpha-2-globin gene (1) 1
alpha-galactosidase a (1) 1
amniocentesis (1) 1
anemia - blood (1) 1
anemia - genetics (1) 1
angiotensin (1) 1
angiotensin-converting enzyme gene polymorphism (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International Journal of Hematology, ISSN 0925-5710, 8/2017, Volume 106, Issue 2, pp. 282 - 290
Journal Article
Journal of the Medical Association of Thailand, ISSN 0125-2208, 09/2018, Volume 101, Issue 9, pp. 1163 - 8
Journal Article
Case Reports in Oncology, ISSN 1662-6575, 05/2017, Volume 10, Issue 2, pp. 769 - 776
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of Cushing syndrome, especially the isolated form without Carney complex, associated... 
Penetrance | Adrenal adenoma | Mutation | Cushing syndrome | Splice site | Adrenal glands | Kinases | Tumors
Journal Article
Journal of Orthopaedic Surgery and Research, ISSN 1749-799X, 09/2011, Volume 6, Issue 1, pp. 47 - 47
Journal Article
Journal of Assisted Reproduction and Genetics, ISSN 1058-0468, 1/2017, Volume 34, Issue 1, pp. 109 - 116
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 2012, Volume 105, Issue 2, pp. S61 - S61
Journal Article
生物医学研究杂志:英文版, ISSN 1674-8301, 2017, Volume 31, Issue 1, pp. 17 - 24
We aimed to explore the prevalence of Fabry disease in Thai patients who were diagnosed with end-stage renal disease(ESRD) of an unknown origin.Venous blood... 
Fabry disease | Alpha-galactosidase A (α-GAL A) | End-stage renal disease (ESRD) | Original | end-stage renal disease (ESRD)
Journal Article
International Journal of Rheumatic Diseases, ISSN 1756-1841, 07/2016, Volume 19, Issue 7, pp. 693 - 699
Journal Article
The Southeast Asian journal of tropical medicine and public health, ISSN 0125-1562, 09/2016, Volume 47, Issue 5, p. 1048
We report, for the first time, hemoglobin (Hb) Lansing-Ramathibodi [α87(F8)His → Gln; CAC>CAG (HBA1: c.264C>G)] in four members of a Thai family presented with... 
Hypoxia - genetics | Hypoxia - pathology | Hemoglobins, Abnormal - genetics | Humans | Hypoxia - etiology | Adult | Family | Female | Male | Thailand
Journal Article
Case Reports in Endocrinology, ISSN 2090-6501, 2014, Volume 2014, pp. 680876 - 7
Background. Fine-needle aspiration (FNA) can cause misdiagnosis of cytomorphological findings between parathyroid and thyroid lesions. Case Presentation. A... 
Bone density | Mutation | Hormones | Genes | Case Report
Journal Article
Journal Article
Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2016, Volume 8, Issue 2
  Thyroid dyshormonogenesis is responsible for 10-15% of all cases of congenital hypothyroidism and is usually inherited. We report a 26-year-old German-Thai... 
Journal Article
Case reports in endocrinology, ISSN 2090-6501, 2013, Volume 2013, pp. 802793 - 4
We report a 26-year-old Thai man who presented with hypoparathyroidism in adulthood. He had no history of cardiac disease and recurrent infection. His subtle... 
Case Report
Journal Article
Southeast Asian Journal of Tropical Medicine and Public Health, ISSN 0125-1562, 2016, Volume 47, Issue 5, pp. 1048 - 1054
We report, for the first time, hemoglobin (Hb) Lansing-Ramathibodi [alpha 87(F8)His -> Gln; CAC>CAG (HBA1: c.264C>G)] in four members of a Thai family... 
HBA1 | Pulse oximetry | Hb Lansing-Ramathibodi | Oxygen saturation | Asians | pulse oximetry | MOLECULAR CHARACTERIZATION | INFECTIOUS DISEASES | ANOMALIES | PHENOTYPE | oxygen saturation | TROPICAL MEDICINE | BONN | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | DECREASED OXYGEN-SATURATION | DISEASE
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.