|1.||Schneider, Holm: 4 articles (09/2015 - 06/2011)|
|2.||Huttner, Kenneth: 4 articles (10/2014 - 06/2011)|
|3.||Johnson, Ramsey: 3 articles (10/2014 - 07/2013)|
|4.||Ye, Xiaoqian: 3 articles (01/2013 - 10/2008)|
|5.||Bian, Zhuan: 3 articles (01/2013 - 10/2008)|
|6.||Yin, Wei: 3 articles (01/2013 - 10/2008)|
|7.||Schneider, Pascal: 3 articles (04/2012 - 11/2007)|
|8.||Casal, Margret L: 3 articles (09/2009 - 07/2005)|
|9.||Shimomura, Yutaka: 2 articles (07/2015 - 01/2011)|
|10.||Kontochristopoulos, George: 2 articles (12/2014 - 09/2007)|
09/01/2009 - "In the study, presented here, we have ascertained two large Pakistani families (A and B) with autosomal recessive form of hypohidrotic ectodermal dysplasia and X-linked recessive isolated hypodontia. "
02/01/2009 - "Recent studies have detected mutations in the EDA gene, previously identified as causing X-linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non-syndromic hypodontia. "
11/01/1980 - "A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia."
01/01/2013 - "Young children with hypodontia caused by hypohidrotic ectodermal dysplasia (HED) not only have difficulties in mastication and speech but can also sense that their appearance is different from others. "
05/01/2012 - "Prosthetic Rehabilitation of a Child Suffering from Hypohidrotic Ectodermal Dysplasia with Complete Anodontia. "
|2.||Anhidrotic Ectodermal Dysplasia 1
08/01/1988 - "This is a report of three patients with hypohidrotic ectodermal dysplasia, or Christ-Siemens-Touraine syndrome, their genealogic backgrounds and the stereomicroscope and scanning electron microscopic appearances of the hair, the skin of their fingertips and palms as well as skin studies of members of their families. "
10/01/2014 - "Christ-Siemens-Touraine syndrome (Hypohidrotic Ectodermal dysplasia (HED)) is a diffuse, non-progressive disease present at birth and involves at least two tissues of ectodermal origin. "
01/01/2012 - "Hypohidrotic ectodermal dysplasia (HED; Christ-Siemens-Touraine syndrome) is a genetic disorder characterized by sparse hair, oligodontia with peg-shaped teeth, reduced sweating, and defects in a number of other ectodermal organs. "
01/01/2009 - "The most common type is hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). "
07/01/2006 - "Christ-Siemens-Touraine syndrome (anhidrotic/hypohidrotic ectodermal dysplasia)."
|3.||Rare Diseases (Rare Disease)
12/01/2009 - "The objective of our study is to precise the epidemioclinical characteristics, the diagnostic tools, the evolution and the treatments of this rare disease through a 10-case series of hypohidrotic ectodermal dysplasia (HED). "
12/01/2011 - "Hypohidrotic ectodermal dysplasia (HED) is a very rare disease characterized by the absence of eccrine glands, dry skin, scanty hair, and dental abnormalities. "
01/01/2006 - "X-linked hypohidrotic ectodermal dysplasia (HED) is a rare disease characterized by the hypoplasia or absence of eccrine glands, dry skin, scant hair, and dental abnormalities. "
09/01/2004 - "Hypohidrotic ectodermal dysplasia (HED) is a very rare disease characterized by the virtual absence of eccrine glands, dry skin, scanty hair, and dental abnormalities. "
|5.||Ectodermal Dysplasia (Aplasia Cutis Congenita)
09/01/2015 - "X-linked hypohidrotic ectodermal dysplasia (XLHED) is the most common form of ectodermal dysplasia. "
10/01/2014 - "X-linked hypohidrotic ectodermal dysplasia (XLHED), the most frequent form of ectodermal dysplasia, is a genetic disorder of ectoderm development characterized by malformation of multiple ectodermal structures such as skin, hair, sweat and sebaceous glands, and teeth. "
09/01/2014 - "Hypohidrotic ectodermal dysplasia (HED) is the most prevalent type of ectodermal dysplasia (ED). "
07/01/2013 - "There are 2 major types of this disorder, based on clinical findings: hypohidrotic ectodermal dysplasia and hidrotic ectodermal dysplasia. "
07/01/2013 - "Hypohidrotic ectodermal dysplasia (HED) is the most common type of ectodermal dysplasia (ED), which encompasses a large group of syndromes that share several phenotypic features such as missing or malformed ectodermal structures, including skin, hair, sweat glands, and teeth. "
|2.||Dental Implants (Dental Implant)
|4.||I-kappa B Kinase
|5.||Type I Tumor Necrosis Factor Receptors
|6.||NF-kappa B (NF-kB)
|7.||Epidermal Growth Factor Receptor (EGF Receptor)
|9.||syndromic 7 Microphthalmia
|10.||Orofaciodigital syndrome type1
|3.||Prostheses and Implants (Prosthesis)
|4.||Vertical Dimension (Occlusion Vertical Dimension)