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Research 61–90 of 1000+
- Inherited Disorders of the Hair
- Veterinary Pharmacology
- Polycystic ovary syndrome and impact on health
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Uncombable hair in a case of Zellweger syndrome – A new association
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”
- Pigmentary mosaicism: An update
- [Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition].
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Acquired pili torti--a structural hair shaft defect in anorexia nervosa.
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Hair removal by lasers and intense pulsed light sources
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Applications of Plasma-Activated Liquid in the Medical Field
- SOX9 in organogenesis: shared and unique transcriptional functions
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Biomedical applications of organoids in genetic diseases
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Oral Retinoids in Dermatology
- Diffuse idiopathic skeletal hyperostosis in a 33-year-old woman with PCOS and metabolic syndrome: a rare scenario
- Oral medications for central serous chorioretinopathy: a literature review
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Clinical Case Notes. Castleman's disease of the lacrimal gland