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Research 451–480 of 1000+
- Dramatic and persistent loss of eyelashes
- Book Reviews
- A rare complication of a common infection
- Hair: more than just an appendage
- Linear lupus panniculitis of scalp: a case report from north-east India
- Pancreatitis associated with valproic acid therapy for epilepsy
- Sodium valproate and thrombocytopenia.
- Finasteride as a therapy for hidradenitis suppurativa
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Recalcitrant alopecia areata responsive to leflunomide and anthralin—Potentially undiscovered JAK/STAT inhibitors?
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Fatal Rapunzel Syndrome
- Queratose folicular espinulosa decalvante: relato de caso
- A Case of Acrodermatitis Enteropathica
- Beyond ECMO Survival: Long-Term Symptom Burden and Quality-of-Life Impairment in Hantavirus Cardiopulmonary Syndrome Survivors
- Trichoscopy and Tinea Capitis: Comma and Corkscrew Hairs
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Trichonodosis: a case report and literature review
- Case Report: Baricitinib improved alopecia areata in a pediatric patient with atopic dermatitis
- A case of alopecia areata after rabies vaccination: unreported adverse effect?
- Alopecia Areata with Renal Dysgenesis
- A Rare association of Mauriac syndrome and Van-Wyk Grumbach syndrome found in a young Saudi girl with poorly controlled type 1 Diabetes and Hypothyroidism: A Case Report and Brief literature review
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- POST-COVID 19 ENCEPHALITIS IN PATIENT WITH DE NOVO MUTATION IN THE SCN1A GENE, A CASE REPORT
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Ulcerative colitis and total alopecia in a mother and her son
- Acrodermatitis Enteropathica‐like Eruption in an Infant with Nonketotic Hyperglycinemia
- Infantile generalized hypertrichosis caused by topical minoxidil
- Circumscribed Alopecia: An Unusual Manifestation of Pediculosis Capitis