Madeleine D Harbison
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Explore the profile of Madeleine D Harbison including associated specialties, affiliations and a list of published articles.
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17
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Recent Articles
1.
Fernandez-Fructuoso J, De la Torre-Sandoval C, Harbison M, Chantot-Bastaraud S, Temple K, Lloreda-Garcia J, et al.
Clin Dysmorphol
. 2021 Sep;
30(4):194-196.
PMID: 34480472
Silver Russell syndrome (SRS) is a congenital disorder characterized by intrauterine growth retardation (IUGR), feeding difficulties and postnatal growth retardation. In a small number of cases, PLAG1 variants have been...
2.
Goodbody C, Buksbaum J, Harbison M, Fragomen A, Rozbruch S
J Pediatr Orthop
. 2021 May;
41(7):428-432.
PMID: 33999566
Introduction: Russell-Silver syndrome (RSS) is a unique cause of syndromic, and often severe, limb length discrepancy (LLD). RSS causes growth retardation both in utero and postnatally, with asymmetry in limb...
3.
Habib W, Brioude F, Azzi S, Rossignol S, Linglart A, Sobrier M, et al.
Sci Adv
. 2019 Feb;
5(2):eaau9425.
PMID: 30801013
Imprinting disorders (IDs) often affect growth in humans, leading to diseases with overlapping features, regardless of the genomic region affected. IDs related to hypomethylation of the human 14q32.2 region and...
4.
Geoffron S, Habib W, Chantot-Bastaraud S, Dubern B, Steunou V, Azzi S, et al.
J Clin Endocrinol Metab
. 2018 Apr;
103(7):2436-2446.
PMID: 29659920
Context: Silver-Russell syndrome (SRS) (mainly secondary to 11p15 molecular disruption) and Temple syndrome (TS) (secondary to 14q32.2 molecular disruption) are imprinting disorders with phenotypic (prenatal and postnatal growth retardation, early...
5.
Salem J, Netchine I, Harbison M
Pediatr Endocrinol Rev
. 2018 Jan;
15(Suppl 1):98-101.
PMID: 29292872
Patient-support organizations can facilitate a significant change in the way rare disorders are approached. Besides connecting families with each other and directing patients to experienced medical specialists, these groups, by...
6.
Heide S, Chantot-Bastaraud S, Keren B, Harbison M, Azzi S, Rossignol S, et al.
J Med Genet
. 2017 Dec;
55(3):205-213.
PMID: 29223973
Background: The 11p15 region contains two clusters of imprinted genes. Opposite genetic and epigenetic anomalies of this region result in two distinct growth disturbance syndromes: Beckwith-Wiedemann (BWS) and Silver-Russell syndromes...
7.
Lemoine A, Harbison M, Salem J, Tounian P, Netchine I, Dubern B
J Pediatr Gastroenterol Nutr
. 2017 Aug;
66(2):306-311.
PMID: 28806298
Objectives: Nutritional management of children with Silver-Russell syndrome (SRS) is crucial, especially before initiating growth hormone therapy. Since cyproheptadine (CYP) has been reported to be orexigenic, we retrospectively investigated the...
8.
Habib W, Brioude F, Edouard T, Bennett J, Lienhardt-Roussie A, Tixier F, et al.
Genet Med
. 2017 Aug;
20(2):250-258.
PMID: 28796236
PurposeFetal growth is a complex process involving maternal, placental and fetal factors. The etiology of fetal growth retardation remains unknown in many cases. The aim of this study is to...
9.
Habib W, Brioude F, Azzi S, Salem J, Das Neves C, Personnier C, et al.
Hum Mutat
. 2016 Oct;
38(1):105-111.
PMID: 27701793
The 11p15 region harbors the IGF2/H19 imprinted domain, implicated in fetal and postnatal growth. Silver-Russell syndrome (SRS) is characterized by fetal and postnatal growth failure, and is caused principally by...
10.
Wakeling E, Brioude F, Lokulo-Sodipe O, OConnell S, Salem J, Bliek J, et al.
Nat Rev Endocrinol
. 2016 Sep;
13(2):105-124.
PMID: 27585961
This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with Silver-Russell syndrome (SRS), an imprinting disorder that causes prenatal and postnatal growth retardation. Considerable overlap exists...