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Research 961–990 of 1000+
- Inherited Acrodermatitis Enteropathica
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Papular atrichia
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Pattern Baldness: Its Genetics Revisited
- Nutrition and hair
- Comparison of Sequential Cyproterone Acetate/Estrogen Versus Spironolactone/Oral Contraceptive in the Treatment of Hirsutism
- Yellow facial papules associated with frontal fibrosing alopecia: A distinct histologic pattern and response to isotretinoin
- Familial Frontal Fibrosing Alopecia Occurs Early in Daughters With Affected Mothers: A Case Report and a Review of the Literature
- Comparative trail on efficacy of topical contact immunotherapy with dinitrochlorobenzene and diphenylcyclopropenone in alopecia areata
- Conflicting Auxin-Phosphate Signals Impact on RSL2 Expression and ROS-Homeostasis Linked to Root Hair Growth in <i>Arabidopsis</i>
- Perspectives of Kennedy's disease
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Congenital adrenal hyperplasia
- Successful induction of oral tolerance in Netherton syndrome
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Hereditary vitamin D rickets: a case series in a family
- Hypotrichosis with juvenile macular dystrophy
- 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
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Congenital and Hereditary Skin Diseases
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report