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Research 451–480 of 1000+
- Inherited Epidermolysis Bullosa: A Clinical Case
- Poster Abstracts
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Azathioprine: A therapy to be considered in alopecia universalis
- Diphencyprone in the treatment of Satoyoshi syndrome
- Dermatological manifestations associated with pregnancy
- Tricotiodistrofia. Reporte de un caso
- Cutaneous manifestations of systemic infection in children
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- The hair shaft: normality, abnormality, and genetics
- Frontal fibrosing alopecia: A multicenter review of 355 patients
- Efficacy and safety of omeprazole for severe gastroesophageal reflux in children
- Genetic prediction of male pattern baldness
- Trichoscopy in Hair Shaft Disorders
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria
- The Genetics of Human Skin Disease
- Contraceptive implant use among inner city teens
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Dermatological Manifestations of Stress in Normal and Psychiatric Populations
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Hair Shaft Dysplasias
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Protective Mechanism of Adipose-Derived Stem Cells in Remodelling of the Skin Stem Cell Niche During Photoaging
- Hair coat characteristics in Friesian heifers in the Netherlands and Kenya : experimental data and a review of literature
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Effects of a new mild shampoo for preventing hair loss in Asian by a simple hand-held phototrichogram technique
- The clinical spectrum of parathyroid disease
- Post-finasteride syndrome – does it really exist?
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients