H Kingston
Overview
Explore the profile of H Kingston including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
180
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Recent Articles
1.
DesLauriers N, Sambai B, Mbogo L, Ludwig-Barron N, Kingston H, Chohan B, et al.
AIDS Behav
. 2023 Jun;
27(12):3970-3980.
PMID: 37318665
We assessed the prevalence and correlates of alcohol use among 870 people who inject drugs living with HIV in Kenya, with attention toward (1) sexual and injecting risk behaviors for...
2.
Madan V, Kingston H, Jamieson L, Goyal N, Ead R
Clin Exp Dermatol
. 2010 May;
35(7):752-5.
PMID: 20456407
We describe a patient with overlapping clinical features of Muckle-Wells syndrome and neonatal-onset multisystem inflammatory disease with an absence of mutation in exon 3 of the CIAS1 ⁄ PYPAF1 ⁄...
3.
Shaikh M, Boyes L, Kingston H, Collins R, Besley G, Padmakumar B, et al.
J Med Genet
. 2008 Sep;
45(9):e1.
PMID: 18762570
Adrenal hypoplasia congenita (AHC) can occur due to deletions or mutations in the DAX 1 (NR0B1) gene on the X chromosome (OMIM 300200). This form of AHC is therefore predominantly...
4.
Slavotinek A, POYSER L, Wallace A, Martin F, Gaunt L, Kingston H
Am J Med Genet A
. 2003 Feb;
117A(3):282-8.
PMID: 12599194
We report two unusual patients with trisomy 18 mosaicism presenting with minor anomalies and failure to thrive in the first year of life. Chromosome analysis showed trisomy 18 in 30/30...
5.
Slavotinek A, Kingston H
J Med Genet
. 2001 Feb;
37(10):796-8.
PMID: 11183187
No abstract available.
6.
Donnai D, Kerzin-Storrar L, Craufurd D, Evans G, Clayton-Smith J, Kingston H
BMJ
. 2000 Sep;
321(7255):241; author reply 242.
PMID: 10979687
No abstract available.
7.
Celli J, van Beusekom E, Hennekam R, Gallardo M, Smeets D, de Cordoba S, et al.
Am J Hum Genet
. 2000 Mar;
66(2):436-44.
PMID: 10677303
Esophageal atresia (EA) is a common life-threatening congenital anomaly that occurs in 1/3,000 newborns. Little is known of the genetic factors that underlie EA. Oculodigitoesophageoduodenal (ODED) syndrome (also known as...
8.
Dodds A, Ramsden R, Kingston H
J Laryngol Otol
. 2000 Feb;
113(10):919-21.
PMID: 10664710
A case of Feingold syndrome is presented with a previously undescribed association of bilateral profound hearing impairment. Computed tomography (CT) scanning revealed severe narrowing of the internal auditory meatuses at...
9.
Slavotinek A, Schwarz C, Getty J, Stecko O, Goodman F, Kingston H
Am J Med Genet
. 1999 Aug;
86(1):75-81.
PMID: 10440834
We present two children with de novo interstitial deletions of the long arm of chromosome 2 (karyotypes 46,XY, del(2)(q31.1q31.3) and 46,XY, del(2)(q24.3q31.3), respectively). The first child had severe learning difficulties,...
10.
Newman B, Meola G, ODonovan D, Schapira A, Kingston H
Neuromuscul Disord
. 1999 Jun;
9(3):144-9.
PMID: 10382907
Proximal myotonic myopathy is a recently described autosomal dominant condition characterized by proximal myopathy, cataracts, intermittent myotonia, and myalgia. We report a further family with this condition. The proband and...