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Research 751–780 of 767
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Uncombable hair in a case of Zellweger syndrome – A new association
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- Addressing Autoimmune and Immune-mediated Skin Disease Burden in Women
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Chronic urticaria versus dermatomyositis in a case of T- cell large granular lymphocytic leukemia
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Alopecia in Belgian Blue crossbred calves: a case series
- Diphenyl cresyl phosphate [MAK Value Documentations, 2003]
- Pharmacogenetics of the Androgen Metabolic Pathway
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- A Cluster of (Old) Portuguese Derivational Suffixes:<i>-ece, -ice, -ez(a),</i>Viewed in Relation to their Spanish Counterparts
- Association of 5α-Reductase Inhibitors With Dementia, Depression, and Suicide
- Polycystic Ovary Syndrome: It’s Not Just Infertility
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Spiny Keratoderma
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- Molecular pathology of skin adnexal tumours
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Inherited Disorders of the Hair
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The human keratins: biology and pathology