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Research 451–480 of 1000+
- Enhancing diagnostic yield of monogenic diabetes through phenotypic and molecular reanalysis of 128 individuals with young onset hyperglycemia: highlighting the significance of accurate case characterization
- A Diagnostic Study of the Prevalence of Helicobacter pylori in Patients with Gastritis in Southern Iraq
- A diagnostic clue: New onset alopecia sparing white hairs
- Navigating diagnostic challenges in syphilitic alopecia: insights from dermoscopy
- The diagnosis and treatment of androgenetic alopecia: a review of the most current management
- From diagnosis to recovery: A practical approach to ringworm treatment in cattle
- Histopathological Diagnosis of Alopecia Clinically Relevant to Alopecia Areata
- CLINICAL DIAGNOSTIC CRITERIA AND COMPLEX THERAPY TELOGENE ALOPECIA IN WOMEN
- Androgenisierung: Diagnostik und Therapie – Akne vulgaris, Hirsutismus, female pattern hair loss
- Clinical diagnosis of COVID-19: a prompt, feasible, and sensitive diagnostic tool for COVID-19 based on a 1,757-patient cohort (The AndroCoV Clinical Scoring for COVID-19 diagnosis).
- Novel diagnostic tools and markers for inflammatory skin diseases
- Clinical diagnosis in canine demodicosis. A new approach.
- The diagnosis and management of alopecia
- A comparison of vertical versus transverse sections for the histopathologic diagnosis of alopecias
- Accuracy of clinical diagnosis and videodermoscopy in female pattern hair loss
- Differential Diagnosis of Male and Female Pattern Hair Loss
- The diagnosis and treatment of iron deficiency and its potential relationship to hair loss
- Early Diagnosis and Prompt Treatment Improves Quality of Life in Patients with Frontal Fibrosing Alopecia
- The Diagnosis and Treatment of Hair and Scalp Diseases
- Office Diagnosis of Hair Shaft Defects
- MicroRNA-21 in Skin Fibrosis: Potential for Diagnosis and Treatment
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- In utero Diagnosis of Trichothiodystrophy by Endoscopically-Guided Fetal Eyebrow Biopsy
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Differential diagnosis of basal cell carcinoma and benign tumors of cutaneous appendages originating from hair follicles by using CD34.
- The diagnosis and treatment of mange in the guinea‐pig caused by <i>Trixacarus (Caviacoptes) caviae</i> (Fain, Hovell & Hyatt, 1972)*
- The diagnosis of androgenetic alopecia in children: Considerations of pathophysiological plausibility
- Hirsutism: Diagnosis and Treatment
- The diagnosis of art: Van Gogh and male pattern baldness