About: Maciej T Malecki

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Polish internist and researcher

Attributes	Values
rdf:type	Item
description	연구원 (ko) araştırmacı (tr) изилдөөчү (ky) onderzoeker (nl) польський дослідник (uk) polski lekarz, internista (pl) Polish internist and researcher (en)
rdfs:label	Maciej Małecki (pl) Maciej T Malecki (en) Maciej T Malecki (nl)
skos:prefLabel	Maciej Małecki (pl) Maciej T Malecki (en) Maciej T Malecki (nl)
name	Maciej Małecki (pl) Maciej T Malecki (en) Maciej T Malecki (nl)
Polish scientist ID (deprecated)	wds:Q89424369-5602a361-4d50-4401-286c-e579d46a9110
Polish scientist ID (deprecated)	85161
given name	wds:Q89424369-0C55C972-6586-452A-890A-A6B881CC9B91 wds:Q89424369-B34EA95B-225B-41C1-896B-8A514F8E3E24
given name	Tadeusz Maciej
instance of	wds:Q89424369-CEDC4465-FF39-4D04-B13A-E8FFD124F4E5
instance of	Homo sapiens
doctoral advisor	wds:Q89424369-AA0146C1-3491-4CD5-A9C9-E5C57253E789
doctoral student	wds:Q89424369-2297457D-103B-41AD-9735-416FA820D9EE wds:Q89424369-24EACA34-60A5-4D4E-BEB9-2E604BA532AE wds:Q89424369-A213E6F9-D976-4EE0-8307-382D8445E40C wds:Q89424369-FAD30F7A-EF59-4B84-9153-585630DF7D8B
doctoral advisor	Jacek Sieradzki
doctoral student	Jan Skupien Katarzyna Cyganek Małgorzata Waluś-Miarka Jerzy Hohendorff
skos:altLabel	Maciej Malecki (en) Maciej Tadeusz Małecki (en) Maciej Tadeusz Małecki (pl)
occupation	wds:Q89424369-F47A3D45-F7DB-4AB3-B4E7-D6C930CF90DD wds:Q89424369-b128f7cc-46f0-adbf-6ae7-3c79a29c74a6 wds:Q89424369-b8693a99-4810-df7e-46d3-e91101694d3f
employer	wds:Q89424369-88DF2E6F-ACED-4655-B01C-DC1282C32F68
NUKAT ID	wds:Q89424369-B62DECEA-D57A-4351-9971-60F78B569C70
sex or gender	wds:Q89424369-63F15F4D-D92F-460C-BA2C-2D57FD043A10
ISNI	wds:Q89424369-57878834-8B5F-4705-BC49-3EE061705D70
VIAF ID	wds:Q89424369-26E88232-AB96-4A2D-A846-A3EAB81BBDB6
academic degree	wds:Q89424369-2BB53032-284D-4225-9604-FA3132E62769 wds:Q89424369-9CC49D79-3C94-42E0-8769-D4CF1789BCC7 wds:Q89424369-C815E17E-031F-481E-ADA9-3C8B21B47F63
date of birth	wds:Q89424369-D2D92824-3053-4FC0-8B96-2C4BBF005C12
educated at	wds:Q89424369-49EA517D-2001-4310-AD09-BEBD8A4757C2
PLWABN ID	wds:Q89424369-6D20F79A-0949-4055-AF09-42D7DA8467EE
family name	wds:Q89424369-EF885B1B-668C-48C0-984E-2E7C77F2CEB9
VIAF ID	http://viaf.org/viaf/311223319
occupation	internist physician researcher
employer	Medical College of Jagiellonian University
NUKAT ID	n2004043674
sex or gender	male
ISNI	0000000111694368
VIAF ID	311223319
academic degree	doctorate habilitation scientific professorship degree
date of birth	1963-01-01 00:00:00Z (xsd:dateTime)
educated at	Medical College of Jagiellonian University
PLWABN ID	9810574238905606
family name	Małecki
ORCID iD	wds:Q89424369-53E27216-A50F-44DC-BE2B-BF6A71A1E686
ORCID iD	https://orcid.org/0000-0002-4794-0820
ORCID iD	0000-0002-4794-0820
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q89424369
is author of	Clinical application of 1,5-anhydroglucitol measurements in patients with hepatocyte nuclear factor-1alpha maturity-onset diabetes of the young Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect Switching to sulphonylureas in children with iDEND syndrome caused by KCNJ11 mutations results in improved cerebellar perfusion Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11. Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood Increased nitric oxide availability attenuates high fat diet metabolic alterations and gene expression associated with insulin resistance Paraoxonase 2 gene C311S polymorphism is associated with a risk of large vessel disease stroke in a Polish population. Monogenic diabetes: implications for therapy of rare types of disease New polymorphism of ENPP1 (PC-1) is associated with increased risk of type 2 diabetes among obese individuals Systematic review and meta-analysis of randomized clinical trials comparing efficacy and safety outcomes of insulin glargine with NPH insulin, premixed insulin preparations or with insulin detemir in type 2 diabetes mellitus A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males. Efficacy and safety of sulfonylurea use in permanent neonatal diabetes due to KCNJ11 gene mutations: 34-month median follow-up Evaluation of Apolipoprotein M Serum Concentration as a Biomarker of HNF-1alpha MODY Type 2 diabetes mellitus and its complications: from the molecular biology to the clinical practice Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses The pseudokinase tribbles homolog 3 interacts with ATF4 to negatively regulate insulin exocytosis in human and mouse beta cells. Genetics of type 2 diabetes mellitus The Pro12Ala polymorphism of PPARγ2 gene and susceptibility to type 2 diabetes mellitus in a Polish population Renal malformations may be linked to mutations in the hepatocyte nuclear factor-1alpha (MODY3) gene Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene Islet-specific antibody seroconversion in patients with long duration of permanent neonatal diabetes caused by mutations in the KCNJ11 gene Synergism between circulating tumor necrosis factor receptor 2 and HbA(1c) in determining renal decline during 5-18 years of follow-up in patients with type 1 diabetes and proteinuria. Homozygous combination of calpain 10 gene haplotypes is associated with type 2 diabetes mellitus in a Polish population Obesity--insulin resistance--type 2 diabetes mellitus Diabetic pregnancy: an overview of current guidelines and clinical practice

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