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Research 781–810 of 1000+
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- A rare case of Vitamin D dependent rickets type II: a case report
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency epidemiology, etiopathogenesis, clinical presentation, treatment – a systematic review
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- Nonclassic congenital adrenal hyperplasia
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- 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
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Papular atrichia
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- 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
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Congenital and Hereditary Skin Diseases