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Research 511–540 of 1000+
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Cutaneous Manifestations of COVID-19: A Brief Review of a Possible Diagnostic Tool
- Eclipta prostrata (L.) L. (Asteraceae): Ethnomedicinal Uses, Chemical Constituents, and Biological Activities
- Androgenetic, Diffuse and Senescent Alopecia in Men: Practical Evaluation and Management
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- AN UPDATED OVERVIEW OF POLYCYSTIC OVARY SYNDROME
- Updates In The Pathogenesis Of Alopecia Areata
- News in brief
- PREFACE
- Book review
- Male Androgenetic Alopecia — Endotext
- Epidemiology and burden of alopecia areata: a systematic review
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- An Overview about Alopecia Areata Etiopathogenesis, Diagnosis, and Management: Review Article
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- P78 Acrodermatitis enteropathica in children: clinical cases
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Identifying critical cell types and gene regulatory pathways for hair and skin disease
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Psoriasis and Related Disorders
- Acne-Associated Syndromes
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Alopecia and its medical management