Search
for
Sort by
Research 421–450 of 1000+
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Recent advances in congenital ichthyoses
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Morphological and inflammatory changes in the skin of autopsied fetuses according to the type of stress
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Hair follicles and their role in skin health
- Two different techniques for frontalis suspension using Gore-Tex to treat severe congenital ptosis
- Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome
- Congenital localized basaloid follicular hamartoma: a case report and review of the literature
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Long-Term Follow-up and Unusual Findings After Microvascular Transfer of Hair-Bearing Skin for Pubic Hair Restoration
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Hiperplasia supra-renal congénita e mielolipoma adrenal - relação causal ou acidental?
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Keratins and skin disease
- The eye and the skin in endocrine metabolic diseases
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome.
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- PSAT097 Patient Preference Research: Preferred Adjunctive Medication Attributes of Adult Patients with Classic Congenital Adrenal Hyperplasia
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Painful thickened skin on the soles of the feet
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita