Search
for
Sort by
Research 451–480 of 1000+
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Type II Vitamin D Dependent Rickets: A Case Report
- Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome
- Inherited Acrodermatitis Enteropathica
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Papular atrichia
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Hypotrichosis with juvenile macular dystrophy
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Congenital adrenal hyperplasia
- Successful induction of oral tolerance in Netherton syndrome
- Hereditary vitamin D rickets: a case series in a family
- Werner′s syndrome
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Congenital and Hereditary Skin Diseases
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Management of pregnancy in a carrier of the Donohue mutation
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- [Netherton's syndrome in two sisters].