Detalhe da pesquisa
1.
SARS-CoV-2 vaccine-associated subacute thyroiditis.
J Endocrinol Invest
; 45(7): 1341-1347, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35182366
2.
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss.
J Eur Acad Dermatol Venereol
; 36(9): 1606-1611, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35543077
3.
Variants in CIB2 cause DFNB48 and not USH1J.
Clin Genet
; 93(4): 812-821, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29112224
4.
LPS-induced Src family kinases activity mediates IL-10 production through activation of STAT3 in peripheral blood mononuclear cells of patients with Behçet's Disease.
Cell Mol Biol (Noisy-le-grand)
; 63(10): 116-121, 2017 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29096751
5.
A Mayan founder mutation is a common cause of deafness in Guatemala.
Clin Genet
; 89(4): 461-465, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26346709
6.
Investigation of the effects of oleuropein rich diet on rat enteric bacterial flora.
Bratisl Lek Listy
; 117(12): 734-737, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-28127972
7.
Prevalence and mutations of ß-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey.
Balkan J Med Genet
; 19(1): 29-34, 2016 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27785405
8.
The MEFV gene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population.
Balkan J Med Genet
; 19(2): 23-28, 2016 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28289585
9.
Vertebrobasilar insufficiency and gamma-glutamyltransferase: An emerging relationship demonstrating inflammation and atherosclerosis.
Bratisl Lek Listy
; 117(8): 448-52, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27546696
10.
Are blood pressure values compatible with medication adherence in hypertensive patients?
Niger J Clin Pract
; 19(4): 460-4, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27251960
11.
Does cerumen have a risk for transmission of HIV?
Eur J Clin Microbiol Infect Dis
; 34(4): 789-93, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25480431
12.
Protective effect of glucagon-like peptide-2 in experimental corrosive esophagitis.
Dis Esophagus
; 28(3): 258-61, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24641662
13.
Attention deficit and hyperactivity disorder and infantile colic.
Minerva Pediatr
; 67(5): 391-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26377777
14.
Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.
Genet Couns
; 25(1): 41-7, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24783654
15.
Relationship between periparturient diseases, metabolic markers and the dynamics of hair cortisol concentrations in dairy cows.
Res Vet Sci
; 158: 134-140, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37004427
16.
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
Clin Genet
; 81(3): 289-93, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21348867
17.
Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation.
Br J Dermatol
; 165(4): 917-21, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21668431
18.
Comprehensive genetic testing can save lives in hereditary hearing loss.
Clin Genet
; 87(2): 190-1, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24689698
19.
A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation.
Clin Genet
; 87(2): 192-5, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702266
20.
Is nerve stimulation needed during an ultrasound-guided lateral sagittal infraclavicular block?
Acta Anaesthesiol Scand
; 54(4): 403-7, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20085542