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Research 121–150 of 1000+
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Epidermal field carcinogenesis in bald-headed: An attempt at finetuning early non-invasive detection
- Maximizing surgical outcomes with gender affirming hormone therapy in gender affirmation surgery
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Necessity of facial contouring in feminization surgery for Chinese transgender females
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- Hair loss among a group of Egyptian children
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- The fundamentals of WNT10A
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Hormonal, Medical, and Nonsurgical Aspects of Gender Affirmation
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Noninflammatory, Nonpruritic Alopecia of Horses
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- [Sodium valproate-induced kinky hair].
- Evaluation of healthcare for transgender veterans
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Dysfunction of keratinocyte adhesion
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- Case Report: Successful Use of Minoxidil to Promote Facial Hair Growth in an Adolescent Transgender Male
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Current Genetics in Hair Diseases
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- SUN-144 Initiating Estradiol Hormone Therapy in a Transgender Woman With Multifocal Idiopathic Localization-Related Epilepsy
- Approach to Alopecia in Dogs in Clinical Practice