Search
for
Sort by
Research 691–720 of 1000+
- Role of Basti in Artavshaya w.s.r. to Lean and Obese Polycystic Ovarian Syndrome
- Woolly hair generalizado: caso clínico e revisão da literatura
- Assessment of Serum Ischemia Modified Albumin Level and Erectile Functions in Individuals with Premature Greying of Hair
- Clinical case of Vogt–Koyanagi–Harada syndrome
- As manifestações dermatológicas da síndrome do ovário policístico: Uma revisão bibliográfica
- Two Incidental Sibling Diagnoses of Netherton Syndrome in Separate Visits: A Case Report
- Association of Obesity and Bariatric Surgery on Hair Health
- Comment on Current Investigations into the Postfinasteride Syndrome
- Alopecia Universalis with Frequently Relapsing Nephrotic Syndrome of Infantile Onset: A Rare Presentation
- Analysis of post-COVID symptoms and predisposing factors for chronic post-COVID syndrome
- The Association of Polycystic Ovarian Syndrome Among Reproductive-Aged Women With Consumption of Junk Food in Jeddah, Saudi Arabia
- SAT320 Cyclic Cushing Syndrome Caused By An ACTH-Producing Pheochromocytoma
- Tourniquet syndrome in children (literature review and own observation)
- Treatment of Alopecia Universalis in a Child with Down Syndrome
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- [Review of the post-COVID-19 syndrome associated to acute telogen effluvium].
- Ayurvedic management of Poly Cystic Ovarian Syndrome (Aarthava Kshaya)
- Polycystic Ovarian Syndrome (PCOS)
- Molecular Basis of Hereditary Hair Diseases
- Cancer risk in polycystic ovary syndrome patients: Common treatments and future perspectives
- Efficacy of Tofacitinib in the Treatment of Universal Alopecia Areata and Primary Sjögren Syndrome
- Secondary amenorrhoea with absent axillary hair
- Uncombable hair improved by biotin
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- IMPACTS OF HYPERANDROGENISM IN MENACMEN WITH POLYCYSTIC OVARY SYNDROME: A LITERATURE REVIEW
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Ocular manifestations of Hutchinson-Gilford-Progeria syndrome: A rare presentation
- Polycystic Ovary Syndrome (PCOS) Presenting with Delayed Menarche and Clitoromegaly
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient