About: Agnieszka Gach

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

Polish clinical geneticist

Attributes	Values
rdf:type	Item
description	연구원 (ko) wetenschapper (nl) дослідниця (uk) Polish clinical geneticist (en) polska lekarka, genetyk kliniczna (pl)
rdfs:label	Agnieszka Gach (ca) Agnieszka Gach (cs) Agnieszka Gach (en) Agnieszka Gach (gl) Agnieszka Gach (hr) Agnieszka Gach (it) Agnieszka Gach (nl) Agnieszka Gach (pl) Agnieszka Gach (ro) Agnieszka Gach (sk) Agnieszka Gach (sl) Agnieszka Gach (hsb) Agnieszka Gach (ast)
skos:prefLabel	Agnieszka Gach (ca) Agnieszka Gach (cs) Agnieszka Gach (en) Agnieszka Gach (gl) Agnieszka Gach (hr) Agnieszka Gach (it) Agnieszka Gach (nl) Agnieszka Gach (pl) Agnieszka Gach (ro) Agnieszka Gach (sk) Agnieszka Gach (sl) Agnieszka Gach (hsb) Agnieszka Gach (ast)
name	Agnieszka Gach (ca) Agnieszka Gach (cs) Agnieszka Gach (en) Agnieszka Gach (gl) Agnieszka Gach (hr) Agnieszka Gach (it) Agnieszka Gach (nl) Agnieszka Gach (pl) Agnieszka Gach (ro) Agnieszka Gach (sk) Agnieszka Gach (sl) Agnieszka Gach (hsb) Agnieszka Gach (ast)
Polish scientist ID (deprecated)	wds:Q91126457-F6D71168-D441-4A36-8C01-750915B6F972
Polish scientist ID (deprecated)	223163
Scopus author ID	wds:Q91126457-384AD151-D3BB-430C-801D-DB918EF641E7
Scopus author ID	57250701100
given name	wds:Q91126457-C608A871-968F-48D3-90E0-D7DA4F751BD3
given name	Agnieszka
instance of	wds:Q91126457-BB6E4348-B425-4DAA-8A30-39BBF2C28801
instance of	Homo sapiens
doctoral advisor	wds:Q91126457-AB5AFD26-1C0C-4CD4-8B06-59F8683F0A8E
doctoral advisor	Wojciech Młynarski
native language	wds:Q91126457-2388C179-A5CC-42C6-B131-0D4F05A88A84
occupation	wds:Q91126457-EB6B4F56-DDE1-4EAE-A16B-65E284EA9DDD
employer	wds:Q91126457-25320BD9-E003-4945-ACA5-DE38B2D68E9D
languages spoken, written or signed	wds:Q91126457-7951CFEB-D5B4-4856-8F4F-CD9E9DDB76C1
name in native language	wds:Q91126457-A04602B9-D0D8-4CEB-AAF9-3FEB7989D72C
sex or gender	wds:Q91126457-A897DEEA-DD6E-408F-81B6-1D6DDAF1F79F
VIAF ID	wds:Q91126457-7CAFF32A-55BF-4B93-95A5-4915289FD040
country of citizenship	wds:Q91126457-491600D0-1605-4DF6-B8CE-A1179970307E
academic degree	wds:Q91126457-379DC70E-B4CA-4F2B-B652-B112E4F945E3 wds:Q91126457-CA65E632-A858-4690-9619-908851C8A442
family name	wds:Q91126457-EE7F85B5-7432-4F07-B829-87EB57467AA0
VIAF ID	http://viaf.org/viaf/313522599
native language	Polish
occupation	researcher
employer	Institute of the Polish Mother's Health Center in Łódź
languages spoken, written or signed	Polish
name in native language	Agnieszka Gach (pl)
sex or gender	female organism
VIAF ID	313522599
country of citizenship	Poland
academic degree	doctorate habilitation
family name	Gach
ORCID iD	wds:Q91126457-667659DC-C0C2-4864-9CB3-4FFFDC5020D6
ORCID iD	https://orcid.org/0000-0002-6590-5797
ORCID iD	0000-0002-6590-5797
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q91126457
is author of	Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11. Efficacy and safety of sulfonylurea use in permanent neonatal diabetes due to KCNJ11 gene mutations: 34-month median follow-up Selective loss of fine tuning of Gq/11 signaling by RGS2 protein exacerbates cardiomyocyte hypertrophy Islet-specific antibody seroconversion in patients with long duration of permanent neonatal diabetes caused by mutations in the KCNJ11 gene The cross-reactivity of anti-asparaginase antibodies against different L-asparaginase preparations Neonatal diabetes in a child positive for islet cell antibodies at onset and Kir6.2 activating mutation Double hit of NEMO gene in preeclampsia Finding NEMO in preeclampsia. Familial partial lipodystrophy as differential diagnosis of polycystic ovary syndrome. The first case report of sulfonylurea use in a woman with permanent neonatal diabetes mellitus due to KCNJ11 mutation during a high-risk pregnancy. Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating [corrected] mutations: evidence for improvement in insulin sensitivity Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea. Association of Maternal and Fetal Single-Nucleotide Polymorphisms in Metalloproteinase (MMP1, MMP2, MMP3, and MMP9) Genes with Preeclampsia. Broad phenotypic spectrum of germline 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia Placental Expression of NEMO Protein in Normal Pregnancy and Preeclampsia The level of extracellular superoxide dismutase in the first week of life in very and extremely low birth weight infants and the risk of developing bronchopulmonary dysplasia "Apple does not fall far from the tree" - subclinical atherosclerosis in children with familial hypercholesterolemia Assessment of insulin sensitivity in adults with permanent neonatal diabetes mellitus due to mutations in the KCNJ11 gene encoding Kir6.2.

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