Search
for
Sort by
Research 121–150 of 1000+
- Atrichia With Papular Lesions
- Epidermal hyperplasia and oral carcinoma in mice overexpressing the transcription factor ATF3 in basal epithelial cells
- Ectodysplasin research—Where to next?
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Store-operated calcium channels in skin
- Noninflammatory, Nonpruritic Alopecia of Horses
- Scaling dermatosis in three dogs associated with abnormal sebaceous gland differentiation
- The Roles of EDA2R in Ageing and Disease
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- A clinician's approach to canine alopecia
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Methotrexate for induction of remission in ulcerative colitis
- EFFECT OF POTASSIUM ON BLOOD-SUGAR AND PLASMA-INSULIN LEVELS IN PATIENTS UNDERGOING PERITONEAL DIALYSIS AND HÆMODIALYSIS
- Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Keratin disorders: from gene to therapy
- Trichothiodystrophy
- A new type of pachyonychia congenita.
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Dermatological diseases from a genetic perspective
- [Low dosage retinol and L-cystine combination improve alopecia of the diffuse type following long-term oral administration].
- Amyloid-Associated Alopecia: A Reappraisal Including Its Pathophysiology
- Hereditary, Congenital, and Acquired Alopecias
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Ugreelig hår