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Research 811–840 of 1000+
- Clinical management of patients with<i>ASXL1</i>mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
- Topical prostaglandin f2α analog induced poliosis
- Congenital Triangular Alopecia (Brauer Nevus)
- Lash Ptosis Caused by Latanoprost
- Granuloma annulare associated with Hodgkin's disease
- Systemic lupus erythematosus in a filly.
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Systemic Lupus Erythematosus With Acute Inflammatory Demyelinating Polyneuropathy: A Case Report and Review of the Literature
- Ptosis in childhood
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Morbihan disease and extrafacial lupus miliaris disseminatus faceie: a case report
- Lichen planopilaris with Koebner phenomenon
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Successful management of multiple extrapulmonary complications associated with<i>Rhodococcus equi</i>pneumonia in a foal
- A Case of Virilizing Brenner Tumor in a Postmenopausal Woman With Stromal Androgenic Activity
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Effectiveness of platelet-rich plasma in long-lasting post-viral olfactory dysfunction: a case-series
- Aching alopecia
- Dermal safety comparison of 0.05% desonide cream and 1.0% hydrocortisone cream
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- An Uncommon and Severe Clinical Case of Sarcoptes scabiei Infestation in a Cat
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Neonatal Occipito-Lınear and Temporo-Fronto-Parıetal Alopecıa: Can Non-Marginal and Marginal forms of the Transient Neonatal Hair Loss be Found Together?
- SUCCESSFUL 28-DAY COMBINATION THERAPY OF MALASSEZIA DERMATITIS IN A 1-YEAR-OLD MIXED SMALL-BREED DOG: A CASE REPORT
- Prospective Evaluation of Topical Minoxidil in Non-Segmental Vitiligo .
- CLINICAL AND DIAGNOSTIC INSIGHTS INTO HYPOTHYROIDISM IN A SHIH-TZU – A CASE REPORT
- Congenital goiter in sibling goat kids