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Research 631–660 of 1000+
- Neurological post‐acute sequelae of SARS‐CoV‐2 infection
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- The diagnosis of androgenetic alopecia in children: Considerations of pathophysiological plausibility
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Clinical, Microscopic and Ultrastructural Findings in a Case of Short Anagen Syndrome
- Cutaneous Manifestations and Hormonal Changes Among Polycystic Ovary Syndrome Patients at a Tertiary Care Center
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Discreet monilethrix: De novo mutation on the example of polish families
- Oncogenic Kras induces spatiotemporally specific tissue deformation through converting pulsatile into sustained ERK activation
- Monilethrix – Case report of a rare disease
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Depression from a physical symptom.
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Recent advances in the epidermal growth factor receptor/ligand system biology on skin homeostasis and keratinocyte stem cell regulation
- Safety Profile of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Disproportionality Analysis of FDA Adverse Event Reporting System
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Continuous MEK inhibition by AZD6244 (ARRY-142886) results in exhaustion of the cutaneous keratinocytic stem cell pool and resembles senescence driven skin aging
- Inherited Acrodermatitis Enteropathica
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Loose anagen syndrome in one identical twin girl
- Hypotrichosis in a child with olmsted syndrome
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Plica Neuropathica in 2 Hispanic Patients
- Clinical Snippets