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Research 301–330 of 1000+
- Hyperplasia of the Subcutaneous Adipose Tissue Is the Primary Histopathologic Abnormality in Lipedematous Scalp
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Short anagen syndrome in a girl with curly dark hair and consanguineous parents
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Overexpression of insulin-like growth factor-1 induces hyperplasia, dermal abnormalities, and spontaneous tumor formation in transgenic mice
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Alopecia in Epidermolysis Bullosa
- Telogen elongation in the hair cycle of <i>ob/ob</i> mice
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Micronutrient status in patients receiving home parenteral nutrition
- Effects of anticonvulsant drugs on chromosomes.
- Cutaneous transcriptome analysis in NIH hairless mice
- Monilethrix: an ultrastructural study
- Topically applied minoxidil may cause fetal malformation: A case report
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Hair Shaft Dysplasias
- Trichothiodystrophy -A Case Report-
- Clinical response of alopecia, trichorrhexis nodosa, and dry, scaly skin to zinc supplementation
- Cardiovascular risk markers in premature canities
- Female pattern baldness in men
- Is prediabetes risk factor for hair loss?
- Hair Changes in Acrodermatitis Enteropathica
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- For early diagnosis of young patients with Werner syndrome: Indication for genetic testing
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Thyroid Autoimmunity in Patients with Skin Disorders
- Trichoscopic Findings of Frontal Fibrosing Alopecia
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin