D J Driscoll
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Explore the profile of D J Driscoll including associated specialties, affiliations and a list of published articles.
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199
Citations
3316
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Recent Articles
1.
Whittington J, Holland A, Driscoll D, Hodebeck-Stuntebeck N, Hoctor A
Orphanet J Rare Dis
. 2022 Feb;
17(1):69.
PMID: 35189933
Background: Prader-Willi syndrome (PWS), is a genetically determined neurodevelopmental disorder, associated with intellectual disabilities and a high incidence of obesity, diabetes mellitus, and respiratory disorders. We hypothesised that COVID-19, a...
2.
Anderson K, Nguyen H, Schoch J, Lohse C, Driscoll D, Tollefson M
J Eur Acad Dermatol Venereol
. 2020 Oct;
35(2):517-522.
PMID: 33070382
Background: Little is known about skin-related complications in Klippel-Trenaunay syndrome (KTS), a complex vascular anomaly defined by capillary malformation (CM), venous malformation (VM) ± lymphatic malformation (LM) and limb overgrowth....
3.
Butler M, Nelson T, Driscoll D, Manzardo A
J Rare Disord
. 2016 Aug;
3(2).
PMID: 27570781
Background: Prader-Willi syndrome (PWS) is a rare obesity-related genetic disorder often caused by a deletion of the chromosome 15q11-q13 region inherited from the father or by maternal disomy 15. Growth...
4.
Miller J, Lynn C, Shuster J, Driscoll D
J Hum Nutr Diet
. 2012 Oct;
26(1):2-9.
PMID: 23078343
Background: Children with Prader-Willi syndrome (PWS) have a predictable pattern of weight gain, with obesity beginning in early childhood and worsening as they get older and hyperphagia increases. Data on...
5.
Khalil A, Driscoll D
Cytogenet Genome Res
. 2010 Jul;
129(4):280-9.
PMID: 20606401
Mammalian meiosis is a process that allows diploid progenitor germ cells to produce haploid gametes after proceeding through 2 rounds of cell divisions. The first division (MI) is unique and...
6.
Hu Y, Li L, Seidelmann S, Timur A, Shen P, Driscoll D, et al.
Ann Hum Genet
. 2008 Jun;
72(Pt 5):636-43.
PMID: 18564129
Klippel-Trenaunay syndrome (KTS) is a severe congenital disorder characterized by capillary malformations, venous malformations or varicose veins, and hypertrophy of the affected tissues. The angiogenic factor gene AGGF1 was previously...
7.
Gloviczki P, Driscoll D
Phlebology
. 2008 Feb;
22(6):291-8.
PMID: 18274338
Klippel-Trenaunay syndrome (KTS) is a rare, sporadic, complex malformation characterized by the clinical triad of (1) capillary malformations (port wine stain); (2) soft tissue and bone hypertrophy or, occasionally, hypotrophy...
8.
Driscoll D
Pediatr Cardiol
. 2007 Sep;
28(6):438-42.
PMID: 17768650
Modifications of the Fontan operation can afford excellent palliation for many patients with a variety of forms of single ventricle. In properly selected patients who are good candidates, early and...
9.
Husmann D, Rathburn S, Driscoll D
J Urol
. 2007 Mar;
177(4):1244-9.
PMID: 17382698
Purpose: Prior reviews regarding genitourinary manifestations of Klippel-Trenaunay syndrome used data acquired from diverse specialty specific articles to define the incidence and sequelae of its genitourinary manifestations. We believe that...
10.
Bartz P, Driscoll D, Keane J, Gersony W, Hayes C, Brenner J, et al.
Pediatr Cardiol
. 2006 Jan;
27(2):259-62.
PMID: 16411151
It is unclear how often patients with very mild aortic stenosis (gradients < 25 mmHg) need interval follow-up. The purpose of this study was to define the determinants of disease...