Search
for
Sort by
Research 601–630 of 1000+
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A new type of pachyonychia congenita.
- 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
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Hypotrichosis congenita of Marie Unna
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Non-classic congenital adrenal hyperplasia
- Treatment of unilateral congenital ptosis
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia.
- A case of androgen-secreting adrenal carcinoma with non-classical congenital adrenal hyperplasia
- The Effect of Simvastatin on Plasma Steroid Hormone Levels in Metformin-Treated Women with Non-Classic Congenital Adrenal Hyperplasia
- A newborn presenting with congenital blistering
- Plasma levels of C19 steroid glucuronides in pre-menopausal women with non-classical congenital adrenal hyperplasia
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- Aplasia cutis congenita on lumbosacral area
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia
- A case of congenital pili multigemini
- The Use of Human Dermal Papillae Conditioned Medium (HDPCM) on Aplasia Cutis Congenita in Lower Extremity due to Intrauterine Varicella Infection
- Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia.
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis