Carlos R Sulsona
Overview
Explore the profile of Carlos R Sulsona including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
163
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0
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Recent Articles
1.
Kweh F, Sulsona C, Miller J, Driscoll D
Obes Sci Pract
. 2023 Aug;
9(4):383-394.
PMID: 37546289
Objective: Prader-Willi syndrome (PWS) is the most frequently diagnosed genetic cause of early childhood obesity. Individuals with PWS typically progress through 7 different nutritional phases during their lifetime. The main...
2.
Burnett L, LeDuc C, Sulsona C, Paull D, Rausch R, Eddiry S, et al.
J Clin Invest
. 2016 Dec;
127(1):293-305.
PMID: 27941249
Prader-Willi syndrome (PWS) is caused by a loss of paternally expressed genes in an imprinted region of chromosome 15q. Among the canonical PWS phenotypes are hyperphagic obesity, central hypogonadism, and...
3.
Burnett L, LeDuc C, Sulsona C, Paull D, Eddiry S, Levy B, et al.
Stem Cell Res
. 2016 Oct;
17(3):526-530.
PMID: 27789403
Prader-Willi syndrome (PWS) is a syndromic obesity caused by loss of paternal gene expression in an imprinted interval on 15q11.2-q13. Induced pluripotent stem cells were generated from skin cells of...
4.
Kweh F, Miller J, Sulsona C, Wasserfall C, Atkinson M, Shuster J, et al.
Am J Med Genet A
. 2014 Oct;
167A(1):69-79.
PMID: 25355237
Circulating total ghrelin levels are elevated in older children and adults with Prader-Willi syndrome (PWS). However, the presence or absence of hyperghrelinemia in young children with PWS remains controversial. We...
5.
Falaleeva M, Sulsona C, Zielke H, Currey K, De La Grange P, Aslanzadeh V, et al.
Clin Med Insights Case Rep
. 2013 May;
6:79-86.
PMID: 23700380
Prader-Willi syndrome (PWS) is caused by the loss of RNA expression from an imprinted region on chromosome 15 that includes SNRPN, SNORD115, and SNORD116. Currently, there are no mouse models...
6.
Omara-Opyene A, Moura P, Sulsona C, Bonilla J, Yowell C, Fujioka H, et al.
J Biol Chem
. 2004 Oct;
279(52):54088-96.
PMID: 15491999
The digestive vacuole plasmepsins PfPM1, PfPM2, PfPM4, and PfHAP (a histoaspartic proteinase) are 4 aspartic proteinases among 10 encoded in the Plasmodium falciparum malarial genome. These have been hypothesized to...