Search
for
Sort by
Research 571–600 of 1000+
- Queen Anne sign
- [Hypothyroid myopathy in a young adult].
- Clinical and Laboratory Findings in Children with Hashimoto’s Thyroiditis
- 8800 A Case of Hypopituitarism Due to Sheehan Syndrome
- SAT378 Unusual Case of Hirsutism From Prolactinoma Induced Dihydrotestosterone Elevation
- Epidermal Renewal after Treatment of Primary Canine Hypothyroidism using Levothyroxine
- SUN-585 A Case of Atypical Myxedema in Hypothyroidism
- Hereditary, Congenital, and Acquired Alopecias
- Hereditary, Congenital, and Acquired Alopecias
- Hypothyroidism with too Many Associations Case Report
- SUN-364 Panhypopituitarism Induced Ventricular Tachycardia: Hormonal Relationship All Should Keep in Mind
- Thyroid hormones and androgens differentially regulate gene expression in testes and ovaries of sexually mature Silurana tropicalis
- Conundrums of hypothyroidism
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Diffuse Alopecia and Thyroid Atrophy in Sheep
- Selenium’s Role on Thyroid Autoimmunity and Cognitive Dysfunction in Elderly
- Multi-Stage Transcriptome Analysis Revealed the Growth Mechanism of Feathers and Hair Follicles during Induction Molting by Fasting in the Late Stage of Egg Laying
- Laboratory Testing in Telogen Effluvium
- Growth of the Hair
- Endocrine Influences on Hair Growth
- How to Diagnose Hair Loss
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- Screening Guidelines for Thyroid Function in Children With Alopecia Areata
- Refractory Postsurgical Hypothyroidism in Nephrotic Syndrome
- SEXUAL DIMORPHISM IN MAMMALS
- Low Anabolic Profile in Assessing a Patient’s Overall Hair Loss
- Psychosis as a late manifestation of Sheehan’s syndrome
- Testosterone- and Cortisol-Secreting Adrenocortical Oncocytoma: An Unusual Cause of Hirsutism
- A STUDY ON CUTANEOUS MANIFESTATIONS OF HYPOTHYROIDISM IN A TERTIARY HOSPITAL IN SOUTH INDIA
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>