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Research 31–60 of 1000+
- TREATMENT SUCCESS IN THREE ANDEAN BEARS (<i>TREMARCTOS ORNATUS</i>) WITH ALOPECIA SYNDROME USING OCLACITINIB MALEATE (APOQUEL®)
- Suspected Calcinosis Cutis and Demodicosis, Secondary to an Exogenous Steroid Administration in a Dog with Hypoadrenocorticism
- Sertolioma in a Canadian Husky: Relationship between Tumor, Hormones, Neurons and Skin
- Bitemporal Scalp Hair Loss: Differential Diagnosis of Nonscarring and Scarring Conditions.
- Linear immunoglobulin A/immunoglobulin G bullous dermatosis associated with Vogt-Koyanagi-Harada disease
- Idiopathic seasonal alopecia in horse: case report
- Characterization and causal investigations of an alopecia syndrome in Australian fur seals (<i>Arctocephalus pusillus doriferus</i>)
- Congenital Triangular Alopecia (Brauer Nevus)
- DERMATOLOGIC INVESTIGATION OF ALOPECIA IN RHESUS MACAQUES (MACACA MULATTA)
- Paraneoplastic alopecia associated with internal malignancies in the cat
- Cycle pilaire et alopécie X chez le chien
- Temporal Triangular Alopecia: Report of an African‐American Child with TTA Misdiagnosed as Refractory Tinea Capitis
- Focal and Generalized Alopecia
- Hereditary, Congenital, and Acquired Alopecias
- Lack of efficacy of topical latanoprost in the treatment of eyebrow alopecia areata
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Lupus-Associated Knee Pain: An Atypical Presentation of Systemic Lupus Erythematosus in a Young Male
- A Novel Atypical Presentation of Frontal Fibrosing Alopecia Involving the Frontoparietal Scalp
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- LUPUS VASCULITIS
- Navigating Rhupus Complexity
- Cutaneous signs in COVID ‐19 patients: A review
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Lichen planopilaris with Koebner phenomenon
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Skin Manifestations of Rheumatological Diseases
- Congenital goiter in sibling goat kids