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Research 91–120 of 347
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Differential plasma proteome analysis reveals key proteins associated with insulin resistance in acne vulgaris patients
- A Review on Cryptorchidism-Induced Alopecia in Dogs
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Two females with hair loss
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Effects Of Keratin-Gelatin And Basic Fibroblast Growth Factor-Gelatin Composite Film On Open Wound Healing In Dogs And Cats
- Syndromes of Severe Insulin Resistance (SSIRs)
- British Society for Dermatopathology: Summaries of Papers
- National scientific medical meeting 1996 abstracts
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Primary cicatricial alopecia: Recent advances in understanding and management
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Targeted elimination of the follicular label-retaining cells by photo-induced cell killing caused a defect on follicular renewal on mice
- Disease causing homozygous variants in the human hairless gene
- Diseases of Periocular Hair
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Langerin+ Dendritic Cells in Cutaneous Fibrosis: The TGF-β1 Signaling Axis
- SULFUR TREATMENT FOR SCABIOSIS IN LOCAL PUPPY
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Disorders of hair in children