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Research 91–120 of 670
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- Disorders of Keratinization
- - Tumor necrosis factor-alpha inhibitor associated psoriasiform alopecia (drug-induced psoriasiform alopecia)
- Woolly Hair in Two Siblings
- Treatment of Psoriasis vulgaris with a New Retinoic Acid Derivative Ro 10-9359
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- Dysfunction of keratinocyte adhesion
- P029 A case of atypical bullous pemphigoid
- PA05 A rare case of cardiocutaneous syndrome in a young child
- LB1671 Large-scale skin scRNA-seq profiling highlights distinct body site-specific ligand-receptor interactions and pathways in keratinocytes
- 413 DC-HIL+ myeloid-derived suppressor cells are elevated in the peripheral blood and lesional skin of cutaneous lupus patients
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Scorbut atypique associé à une anorexie mentale
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Efficacy and safety of systemic monotherapy in the management of generalized pustular psoriasis: A systematic review
- 415 IL-17C: Checkpoint in innate skin immunology
- [Acitretine].
- [Oral treatment of severe psoriasis with a new aromatic retinoid (Ro 10-9359) (author's transl)].
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Clinicopathological and Immunofluorescence study of Lichen Planus
- Antipsoriatic Activity of a New Synthetic Retinoid
- Dapsone Therapy for Pustular Psoriasis: Case Series and Review of the Literature
- 414 A fitst-in-human study of BLZ-100 (tozuleristide) demonstrates tolerability and fluorescence contrast in skin cancer
- 412 High amphiregulin expression is a high-risk feature of acute graft-versus-host disease of the skin
- Role of caffeine in the management of androgenetic alopecia
- 174 Changes in urine androgen and PG levels during finasteride treatment
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient