Search
for
Sort by
Research 331–360 of 1000+
- Essential syphilitic alopecia: Non-scarring alopecia in 21-year-old man
- Graham-Little-Piccardi-Lassueur Syndrome: Two Case Reports and Review of the Literature
- Anti-DFS70 sebagai Penanda Kejadian Autoimun Nonsistemik (Primary Billiar Cholangitis) pada Systemic Lupus Erythematosus
- MON-024 Steroid Cell Tumor, Not Otherwise Specified; A Rare Case of Hyperandrogenism
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Examination of Clinical and Demographic Characteristics of 14 Cases with Frontal Fibrosing Alopecia
- ANDROGEN AND CORTISOL SECRETING ADRENOCORTICAL ONCOCYTOMA WITTH UNCERTAIN MALIGNANT POTENTIAL
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- 576 Merkel cell carcinoma with fungi infection: A case report
- SAT-224 Polycystic Ovary Syndrome with Adrenal Hyperandrogenemia and Refractory Hirsutism
- Polycystic Ovary Syndrome
- Conundrums of hypothyroidism
- Concurrent hepatitis B and autoimmune hepatitis a rare presentation of acute liver failure: a case report
- Diagnosis and management of pemphigus foliaceus in a dog
- Wanita dengan Sindrom Rupus : Lupus Eritematosus Sistemik dan Artritis Reumatoid
- Fever of unknown origin in a male patient with systemic lupus erythematosus.
- Steroid Cell Tumor Without Virilization
- Frontal fibrosing alopecia
- Research progress on drug-induced gynecomastia
- The Case Files
- Fever, Maculopapular Rash and Severe Aphthous Stomatitis in a Renal Transplant Patient
- Gonads
- Diagnosis by Hair Sample:A Rare Case of Netherton Syndrome in a 2-Year-Old Girl
- Hair loss in women
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Graft versus host disease–like: A new paraneoplastic syndrome
- Hydrochlorothiazide/indometacin
- Klinefelter syndrome and chronic leg ulcers
- Adrenocortical tumor in 20 months old female
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy