Detalhe da pesquisa
1.
Why PRP works only on certain patients with tennis elbow? Is PDGFB gene a key for PRP therapy effectiveness? A prospective cohort study.
BMC Musculoskelet Disord
; 22(1): 710, 2021 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34407802
2.
Uremic pruritus and serum brain-derived neurotrophic factor in diabetic and non-diabetic haemodialysis patients.
Postepy Dermatol Alergol
; 37(6): 932-937, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33603612
3.
Mesenchymal Stem Cells-Potential Applications in Kidney Diseases.
Int J Mol Sci
; 20(10)2019 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31109047
4.
Relationship between CETP gene polymorphisms with coronary artery disease in Polish population.
Mol Biol Rep
; 45(6): 1929-1935, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30178218
5.
Pentoxifylline and Methylprednisolone Additively Alleviate Kidney Failure and Prolong Survival of Rats after Renal Warm Ischemia-Reperfusion.
Int J Mol Sci
; 19(1)2018 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29324683
6.
Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke.
J Stroke Cerebrovasc Dis
; 27(7): 1885-1889, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29598907
7.
The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study.
J Stroke Cerebrovasc Dis
; 26(12): 2763-2768, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28778720
8.
Efficacy of acarbose in different geographical regions of the world: analysis of a real-life database.
Diabetes Metab Res Rev
; 31(2): 155-67, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044702
9.
The rs2516839 Polymorphism of the USF1 Gene May Modulate Serum Triglyceride Levels in Response to Cigarette Smoking.
Int J Mol Sci
; 16(6): 13203-16, 2015 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26068452
10.
Influence of education, marital status, occupation, and the place of living on skeletal status, fracture prevalence, and the course and effectiveness of osteoporotic therapy in women in the RAC-OST-POL Study.
J Bone Miner Metab
; 32(1): 89-95, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23690162
11.
The -930A>G polymorphism of the CYBA gene is associated with premature coronary artery disease. A case-control study and gene-risk factors interactions.
Mol Biol Rep
; 41(5): 3287-94, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24477591
12.
Calcium intake and osteoporosis: the influence of calcium intake from dairy products on hip bone mineral density and fracture incidence - a population-based study in women over 55 years of age.
Public Health Nutr
; 17(2): 383-9, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23217270
13.
Is TCF7L2 variant associated with non-diabetic chronic kidney disease progression? Results of a family-based study.
Postepy Hig Med Dosw (Online)
; 68: 343-9, 2014 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24864085
14.
BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients.
Blood Cells Mol Dis
; 50(1): 33-8, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23040356
15.
Substance P and intensity of pruritus in hemodialysis and peritoneal dialysis patients.
Med Sci Monit
; 19: 723-32, 2013 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23995243
16.
Epidemiological data on osteoporosis in women from the RAC-OST-POL study.
J Clin Densitom
; 15(3): 308-14, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22425509
17.
1936AâG (I646 V) polymorphism in the AKAP10 gene encoding A-kinase-anchoring protein 10 in very long-lived poles is similar to that in newborns.
Exp Aging Res
; 38(5): 584-92, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23092224
18.
[Carbohydrate sweeteners and obesity]. / Weglowodanowe substancje slodzace a otylosc.
Przegl Lek
; 69(4): 157-62, 2012.
Artigo
em Polonês
| MEDLINE | ID: mdl-23029710
19.
Imeglimin: a new antidiabetic drug with potential future in the treatment of patients with type 2 diabetes.
Endokrynol Pol
; 73(2): 361-370, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35381095
20.
Fabry disease - a genetically conditioned extremely rare disease with a very unusual course.
Intractable Rare Dis Res
; 11(1): 34-36, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35261850