Results 31 to 40 of about 1,144,906 (160)

Identification of GJB6 gene mutation in an Indian man with Clouston syndrome

open access: diamondIndian Journal of Dermatology, Venereology, and Leprology, 2016
Nidheesh Agarwal   +4 more
openalex   +2 more sources

Clouston’s Syndrome-A Case Report

open access: yesAnnals of King Edward Medical University, 2021
A heterogeneous group of disorders namely Clouston’s syndromes characterized by a primary defect in teeth, hair, nail and sweat glands with an estimated frequency of about seven per 10,000 births. Hidrotic ectodermal dysplasia or Clouston syndrome is a rare inherited disorder of ectodermal dysplasia.
Ghazala Butt   +5 more
openaire   +1 more source

Causal Variants of the GJB6 Gene are Associated with Hearing Loss and Skin Manifestations: A Case Report from Turkey

open access: yesInternational Journal of Dermatology and Venerology, 2022
Introduction:. The gap junction beta 6 (GJB6) gene encodes connexin 30. This protein plays critical role in tissues and is responsible for the formation of gap junctions, which have a wide variety of physiological functions.
Neslihan Duzkale   +4 more
doaj   +1 more source

Rehabilitation with implant‐supported overdentures in preteens patients with ectodermal dysplasia: A cohort study

open access: yesClinical Implant Dentistry and Related Research, Volume 25, Issue 6, Page 1187-1196, December 2023., 2023
Abstract Introduction Hypohidrotic ectodermal dysplasia (HED) patients suffering of oligo‐anodontia require early dental treatment to improve oral functions and reduce social impairment. The aim of this study was to evaluate the skeletal growth, implant and prosthetic survival rate, success, and complications after the rehabilitation with a maxillary ...
Marco Montanari   +4 more
wiley   +1 more source

Electrodiagnostic subtyping in Guillain‐Barré syndrome: Use of criteria in practice based on a survey study in IGOS

open access: yesJournal of the Peripheral Nervous System, Volume 27, Issue 3, Page 197-205, September 2022., 2022
Abstract Electrodiagnostic (EDx) studies are helpful in diagnosing and subtyping of Guillain‐Barré syndrome (GBS). Published criteria for differentiation into GBS subtypes focus on cutoff values, but other items receive less attention, although they may influence EDx subtyping: (a) extensiveness of EDx testing, (b) nerve‐specific considerations, (c ...
Samuel Arends   +17 more
wiley   +1 more source

Inequality in early life: Social class differences in childhood mortality in southern Sweden, 1815–1967

open access: yesThe Economic History Review, Volume 75, Issue 2, Page 475-502, May 2022., 2022
Abstract This article analyses the long‐term development of social class differences in infant and child mortality in an area of southern Sweden, spanning from the early stages of the mortality transition at the beginning of the nineteenth century, to the late 1960s when both infant and child mortality had reached very low levels.
Martin Dribe, Omar Karlsson
wiley   +1 more source

Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group

open access: yesLiver International, Volume 42, Issue 5, Page 1058-1069, May 2022., 2022
Abstract Background & Aims Diagnostic histological criteria for autoimmune hepatitis (AIH) have not been clearly established. Previously published criteria focused mainly on chronic AIH, in which inflammatory changes mainly occur in portal/periportal regions and may not be applicable to acute presentation of AIH, in which inflammatory changes are ...
Ansgar W. Lohse   +18 more
wiley   +1 more source

The World Trade Center Health Program: Twenty years of health effects research

open access: yesAmerican Journal of Industrial Medicine, Volume 64, Issue 10, Page 797-802, October 2021., 2021
Abstract It has been 20 years since the devastating terrorist attacks on September 11, 2001. Thousands were injured or killed during the attacks and many more are at risk of adverse health stemming from physical, psychological, and emotional stressors born out of the attacks.
Robert D. Daniels   +3 more
wiley   +1 more source

Presentation of hypohidrotic ectodermal dysplasia in two siblings

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2015
Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-linked recessive disorders and have a full expression in males, whereas females show little to no signs of the disorder.
Uday Ginjupally   +3 more
doaj   +1 more source

[Selected publications] [PDF]

open access: yes, 1921
01. MANURIAL EXPERIMENTS WITH WHEAT AT THE NAGPUR EXPERIMENTAL FARM by D, CLOUSTON (reprìnted from the AGRICULTURAL JOURNAL OF INDIA, VOL I., PART III. 1906) || 02. ARTIFICIAL FERTILIZERS FOR COTTON, CENTRAL PROVINCES AND BERAR by D.
Clouston, D.
core   +3 more sources

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