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Research 121–150 of 1000+
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Ulerythema ophryogenes with multiple congenital anomalies
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- “Case Report : Early Congenital Syphilis”
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- FOXN1 deficient nude severe combined immunodeficiency
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Dermatopathology and molecular genetics
- Leptomeningeal angiomatosis accompanied by hair follicle nevus
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Side effects after artificial hair implants: 2 case reports
- Nevus psiloliparus: Newly described histopathological features from transverse sections
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Hair loss disorders in domestic animals
- Le gène<i>hairless</i>de la souris
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis