Moris Angulo
Overview
Explore the profile of Moris Angulo including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
222
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Miller J, Gevers E, Bridges N, Yanovski J, Salehi P, Obrynba K, et al.
Obesity (Silver Spring)
. 2023 Nov;
32(2):252-261.
PMID: 37919617
Objective: This study assessed the effect of 1-year administration of diazoxide choline extended-release tablet (DCCR) on hyperphagia and other complications of Prader-Willi syndrome (PWS). Methods: The authors studied 125 participants...
2.
Miller J, Gevers E, Bridges N, Yanovski J, Salehi P, Obrynba K, et al.
J Clin Endocrinol Metab
. 2023 Jan;
108(7):1676-1685.
PMID: 36639249
Context: Prader-Willi syndrome (PWS) is a rare neurobehavioral-metabolic disease caused by the lack of paternally expressed genes in the chromosome 15q11-q13 region, characterized by hypotonia, neurocognitive problems, behavioral difficulties, endocrinopathies,...
3.
Liraglutide for Weight Management in Children and Adolescents With Prader-Willi Syndrome and Obesity
Diene G, Angulo M, Hale P, Jepsen C, Hofman P, Hokken-Koelega A, et al.
J Clin Endocrinol Metab
. 2022 Oct;
108(1):4-12.
PMID: 36181471
Context: Prader-Willi syndrome (PWS) is characterized by lack of appetite control and hyperphagia, leading to obesity. Pharmacological options for weight management are needed. Objective: To determine whether liraglutide treatment for...
4.
Angulo M, Abuzzahab M, Pietropoli A, Ostrow V, Kelepouris N, Tauber M
Int J Pediatr Endocrinol
. 2020 Dec;
2020(1):20.
PMID: 33292530
Background: Growth hormone (GH) deficiency is common in patients with Prader-Willi syndrome (PWS) and leads to short adult stature. The current study assessed clinical outcomes based on real-world observational data...
5.
Singh D, Sasson A, Rusciano V, Wakimoto Y, Pinkhasov A, Angulo M
Am J Med Genet A
. 2019 May;
179(7):1241-1245.
PMID: 31070005
Psychosis is a relatively common psychiatric phenomenon seen in patients with Prader-Willi Syndrome (PWS). However, the presentation is atypical and difficult to classify within currently defined affective or psychotic disorders....
6.
Singh D, Wakimoto Y, Filangieri C, Pinkhasov A, Angulo M
J Child Adolesc Psychopharmacol
. 2019 Feb;
29(4):313-317.
PMID: 30724590
To examine the role of Guanfacine Extended Release (GXR) in the management of behavioral disturbances in patients with Prader-Willi Syndrome (PWS). Twenty from a total of 27 individuals with genetically...
7.
Dykens E, Miller J, Angulo M, Roof E, Reidy M, Hatoum H, et al.
JCI Insight
. 2018 Jun;
3(12).
PMID: 29925684
Background: Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder of life-threatening hyperphagia, obesity, intellectual deficits, compulsivity, and other behavioral problems. The efficacy and safety of i.n. carbetocin, an oxytocin analog,...
8.
McCandless S, Yanovski J, Miller J, Fu C, Bird L, Salehi P, et al.
Diabetes Obes Metab
. 2017 May;
19(12):1751-1761.
PMID: 28556449
Aims: There are no treatments for the extreme hyperphagia and obesity in Prader-Willi syndrome (PWS). The bestPWS clinical trial assessed the efficacy, safety and tolerability of the methionine aminopeptidase 2...
9.
Miller J, Angulo M
Am J Med Genet A
. 2013 Dec;
164A(2):421-4.
PMID: 24311388
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by an abnormality on the long arm of chromosome 15 (q11-q13) that results in a host of behavioral characteristics including excessive...
10.
Cataletto M, Angulo M, Hertz G, Whitman B
Int J Pediatr Endocrinol
. 2011 Oct;
2011(1):12.
PMID: 22008714
The advent of sensitive genetic testing modalities for the diagnosis of Prader-Willi syndrome has helped to define not only the phenotypic features of the syndrome associated with the various genotypes...