Search
for
Sort by
Research 391–420 of 1000+
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- AORTOCAVAL PARAGANGLIOMA IN VON HIPPEL-LINDAU DISEASE
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- The Case | Bilateral kidney tumors and lung cysts
- Clinical Snippets
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- A Current Diagnostic and Therapeutic Challenge: Tinea Capitis
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- GLABROUS INFLORESCENCE STEMS3 binds to and activates <i>RHD2</i> and <i>RHD4</i> genes to promote root hair elongation in Arabidopsis
- Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report
- Social selection favours offspring prone to the development of androgenetic alopecia.
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- 8242 A Case of Ayme Gripp Syndrome
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Salt-losing tubulopathy and chronic dermatitis
- The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Badanie roli zmienności genetycznej i epigenetycznej w starzeniu się skóry twarzy i włosów głowy oraz genetyczna predykcja związanych z wiekiem cech wyglądu człowieka
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- Kératose pilaire
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- Novel insights into cardiocutaneous syndromes