Carlos Knopf
Overview
Explore the profile of Carlos Knopf including associated specialties, affiliations and a list of published articles.
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Articles
10
Citations
238
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0
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Recent Articles
1.
Dumin E, Faour Z, Knopf C, Spiegel R, Elisha M, Kaplan M, et al.
J Neuromuscul Dis
. 2016 Nov;
2(s1):S40.
PMID: 27858634
No abstract available.
2.
Blumenfeld Z, Kaidar G, Zuckerman-Levin N, Dumin E, Knopf C, Hochberg Z
Clin Med Insights Reprod Health
. 2016 May;
10:9-13.
PMID: 27168731
Objective: The aim of this study was to assess the activity of cortisol-metabolizing enzymes in women with polycystic ovary syndrome (PCOS), using a fully quantitative gas chromatography/mass spectrometry (GCMS) method....
3.
Lefeber D, de Brouwer A, Morava E, Riemersma M, Schuurs-Hoeijmakers J, Absmanner B, et al.
PLoS Genet
. 2012 Jan;
7(12):e1002427.
PMID: 22242004
Genetic causes for autosomal recessive forms of dilated cardiomyopathy (DCM) are only rarely identified, although they are thought to contribute considerably to sudden cardiac death and heart failure, especially in...
4.
Zuckerman-Levin N, Tsivlin L, Knopf C, Flor O, Shen-Orr Z, Levin M, et al.
Pediatr Res
. 2011 May;
70(2):208-12.
PMID: 21544007
Small for GA (SGA) children are at risk for developing the metabolic syndrome. Those who do not catch up, and remain short (SSGA), may benefit from GH therapy. 11β Hydroxysteroid...
5.
Basel-Vanagaite L, Sarig O, Hershkovitz D, Fuchs-Telem D, Rapaport D, Gat A, et al.
Am J Hum Genet
. 2009 Jul;
85(2):254-63.
PMID: 19631308
Inherited disorders of elastic tissue represent a complex and heterogeneous group of diseases, characterized often by sagging skin and occasionally by life-threatening visceral complications. In the present study, we report...
6.
Tiosano D, Knopf C, Koren I, Levanon N, Hartmann M, Hochberg Z, et al.
Eur J Endocrinol
. 2008 Feb;
158(3):385-92.
PMID: 18299473
Context: The CYP17A1 gene encodes many enzymatic reactions including 17alpha-hydroxylase and 17,20-lyase activities. Mutations that selectively ablate the 17,20-lyase activity, causing isolated 17,20-lyase deficiency, are exceedingly rare and may belong...
7.
Mandel H, Shemer R, Borochowitz Z, Okopnik M, Knopf C, Indelman M, et al.
Am J Hum Genet
. 2008 Jan;
82(1):39-47.
PMID: 18179883
The WNT-signaling pathway plays a major role during mammalian embryogenesis. We report a novel autosomal-recessive syndrome that consists of female to male sex reversal and renal, adrenal, and lung dysgenesis...
8.
Iancu T, Mahajnah M, Manov I, Cherurg S, Knopf C, Mandel H
Ultrastruct Pathol
. 2007 Jul;
31(3):189-97.
PMID: 17613998
A new group of genetic diseases characterized by defective glycoprotein biosynthesis was recently described. Transferrin isoelectric focusing enabled identification of several types of patients with congenital disorders of glycosylation (CDG)....
9.
Adiv O, Mandel H, Shehadeh N, Knopf C, Shen-Or Z, Shamir R
J Nutr Biochem
. 2004 Nov;
15(10):638-43.
PMID: 15542356
Insulin and docosahexaenoic acid are both present in human milk. The aim of this study was to examine the effect of co-administration of oral insulin and DHA in mice. Immediately...
10.
Kaplan M, Aviram M, Knopf C, Keidar S
Biochem Biophys Res Commun
. 2002 Feb;
290(5):1529-34.
PMID: 11820795
Impaired cellular cholesterol efflux in cells of the arterial wall is suggested to be involved in the pathogenesis of atherosclerosis. Since angiotensin II (Ang-II) is implicated in the development of...