Search
for
Sort by
Research 931–960 of 1000+
- Episodic Bilateral Corneal Edema Caused by Hair Groom Gel
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Growing Up Fast: Managing Autism Spectrum Disorder and Precocious Puberty
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- Reply
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Epithelial elements in superficial angiomyxomas: mimicry of adnexal development, and mesenchymal‐to‐epithelial transition
- Fgf21 Deficiency Delays Hair Follicle Cycling and Modulates miRNA–Target Gene Interactions in Mice
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation
- An unusual case of Anasarca-Rapunzel syndrome
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- PCSK9: From Nature’s Loss to Patient’s Gain
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
- Uncombable hair in a case of Zellweger syndrome – A new association