Peter Heydemann
Overview
Explore the profile of Peter Heydemann including associated specialties, affiliations and a list of published articles.
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21
Citations
572
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Recent Articles
1.
Neul J, Benke T, Marsh E, Suter B, Fu C, Ryther R, et al.
Genes (Basel)
. 2024 Aug;
15(8).
PMID: 39202466
Although long-term survival in Rett syndrome (RTT) has been observed, limited information on older people with RTT exists. We hypothesized that increased longevity in RTT would be associated with genetic...
2.
Felin M, Wang K, Raggi C, Moreira A, Pandey A, Grose A, et al.
Curr Pediatr Rep
. 2023 Sep;
10(3):109-124.
PMID: 37744780
Purpose Of Review: Review comprehensive data on rates of toxoplasmosis in Panama and Colombia. Recent Findings: Samples and data sets from Panama and Colombia, that facilitated estimates regarding seroprevalence of...
3.
Felin M, Wang K, Moreira A, Grose A, Leahy K, Zhou Y, et al.
Curr Pediatr Rep
. 2023 Mar;
10(3):93-108.
PMID: 36969368
Purpose Of Review: Review work to create and evaluate educational materials that could serve as a primary prevention strategy to help both providers and patients in Panama, Colombia, and the...
4.
Felin M, Wang K, Moreira A, Grose A, Leahy K, Zhou Y, et al.
Curr Pediatr Rep
. 2022 Aug;
10(3):57-92.
PMID: 36034212
Purpose Of Review: Review building of programs to eliminate infections. Recent Findings: Morbidity and mortality from toxoplasmosis led to programs in USA, Panama, and Colombia to facilitate understanding, treatment, prevention,...
5.
Felin M, Wang K, Moreira A, Grose A, Leahy K, Zhou Y, et al.
Curr Pediatr Rep
. 2022 Aug;
10(3):125-154.
PMID: 35991908
Purpose Of Review: Review international efforts to build a global public health initiative focused on toxoplasmosis with spillover benefits to save lives, sight, cognition and motor function benefiting maternal and...
6.
Fang X, Butler K, Abidi F, Gass J, Beisang A, Feyma T, et al.
Mol Genet Genomic Med
. 2022 Mar;
10(5):e1917.
PMID: 35318820
Background: Rett syndrome (RTT) is a rare neurodevelopmental disorder associated with pathogenic MECP2 variants. Because the MECP2 gene is subject to X-chromosome inactivation (XCI), factors including MECP2 genotypic variation, tissue...
7.
Motil K, Geerts S, Annese F, Neul J, Benke T, Marsh E, et al.
J Pediatr
. 2022 Jan;
244:169-177.e3.
PMID: 35063470
Objective: To characterize growth and anthropometric measurements in females with Rett syndrome and compare these measurements with functional outcomes. Study Design: We obtained longitudinal growth and anthropometric measurements from 1154...
8.
Mitelman O, Abdel-Hamid H, Byrne B, Connolly A, Heydemann P, Proud C, et al.
J Neuromuscul Dis
. 2021 Aug;
9(1):39-52.
PMID: 34420980
Background: Studies 4658-201/202 (201/202) evaluated treatment effects of eteplirsen over 4 years in patients with Duchenne muscular dystrophy and confirmed exon-51 amenable genetic mutations. Chart review Study 4658-405 (405) further...
9.
Raspa M, Bann C, Gwaltney A, Benke T, Fu C, Glaze D, et al.
Am J Intellect Dev Disabil
. 2020 Nov;
125(6):493-509.
PMID: 33211820
Rett syndrome (RTT) is a neurodevelopmental disorder that primarily affects females. Recent work indicates the potential for disease modifying therapies. However, there remains a need to develop outcome measures for...
10.
Neul J, Skinner S, Annese F, Lane J, Heydemann P, Jones M, et al.
Front Integr Neurosci
. 2020 Mar;
14:7.
PMID: 32161522
Rett syndrome (RTT, OMIM 312750), a severe neurodevelopmental disorder characterized by regression with loss of spoken language and hand skills, development of characteristic hand stereotypies, and gait dysfunction, is primarily...