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Research 121–150 of 1000+
- β-Catenin Signaling Increases in Proliferating NG2+ Progenitors and Astrocytes during Post-Traumatic Gliogenesis in the Adult Brain
- Effects of Fetal Exposure to Diazoxide in Man
- Prematurity: is it a risk factor for striae distensae?
- Polycystic ovarian syndrome: Prevalence and its correlates among adolescent girls
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Sexual difference, identification and object choice in individuals with sex differentiation disorders
- Targeted overexpression of parathyroid hormone-related peptide in chondrocytes causes chondrodysplasia and delayed endochondral bone formation.
- Two parietal cephaloceles in a female neonate
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Erosive Pustular Dermatosis of the Scalp after Perinatal Scalp Injury
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital Atrichia: A Case Report
- US Preterm Births: “D” Is for Dismal
- Spontaneous Pathology of Endangered Geriatric Julia Creek Dunnarts (<em>Sminthopsis douglasi</em>, Archer 1979) with Emphasis in Reproductive Pathology
- Biotinidase deficiency – clinching the diagnosis rapidly can make all the difference!
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Ethnic Hair Considerations for People of African, South Asian, Muslim, and Sikh origins
- Congenital goiter in sibling goat kids
- H03 Madam C.J. Walker and her wonderful hair grower
- Hypotrichosis congenita of Marie Unna
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Alopecia side-effect of antituberculosis drugs
- Cyproterone acetate and risk of meningioma: a nationwide cohort study
- Congenital atrichia associated with situs inversus and mesocardia