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Research 211–240 of 599
- Impaired Fetal Lung Development can be Rescued by Administration of Extracellular Vesicles Derived from Amniotic Fluid Stem Cells
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- 46,XY DSD due to impaired androgen production
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature
- AMINOPTERIN IN TREATMENT OF LEUKEMIA IN CHILDREN
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Congenital atrichia with papular lesions
- Congenital hypotrichosis in a French bulldog
- SAT-214 Satoyoshi Syndrome: A Rare Cause of Premature Ovarian Failure
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Induction of Pluripotent Stem Cells Via Wnt Signaling Pathway.
- 169 Red Sky in Morning: A Case of Concurrent Hematospermia and Anorgasmia
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Defining the identity of mouse embryonic dermal fibroblasts
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Satoyoshi Syndrome: Difficult to find or treat?
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>