Detalhe da pesquisa
1.
Intima media thickness of common carotids and abdominal aorta in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in relation to their genotypes.
Neuro Endocrinol Lett
; 38(3): 154-162, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28759182
2.
Circadian blood pressure profiles and ambulatory arterial stiffness index in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in relation to their genotypes.
Neuro Endocrinol Lett
; 38(7): 509-518, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29369603
3.
The role of polymorphisms of genes encoding collagen IX and XI in lumbar disc disease.
Neurol Neurochir Pol
; 48(1): 60-2, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24636772
4.
New insights into thyroid dysfunction in patients with inactivating parathyroid hormone/parathyroid hormone-related protein signalling disorder (the hormonal and ultrasound aspects): One-centre preliminary results.
Front Endocrinol (Lausanne)
; 13: 1012658, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36213284
5.
[Fetal CD34+ cells isolated from maternal blood and cytogenetics array as potential tools in screening, non-invasive prenatal diagnosis--preliminary research]. / Plodowe komórki CD34+ izolowane z krwi matki oraz mikromacierze cytogenetyczne jako potencjalne narzedzia w przesiewowej, nieinwazyjnej diagnostyce prenatalnej--badania wstepne.
Przegl Lek
; 68(1): 40-3, 2011.
Artigo
em Polonês
| MEDLINE | ID: mdl-21563443
6.
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital Microcephaly.
Genes (Basel)
; 12(12)2021 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34946966
7.
Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types I or III.
Acta Biochim Pol
; 65(1): 79-86, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29543922
8.
Novel pathogenic variant in the HRAS gene with lethal outcome and a broad phenotypic spectrum among Polish patients with Costello syndrome.
Clin Dysmorphol
; 26(2): 83-90, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28027064