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Research 61–90 of 1000+
- Photobiomodulation therapy
- Psychocutaneous disease
- Alopecia and Periodontitis: Exploring the connecting dots
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Syndromes of Severe Insulin Resistance (SSIRs)
- <i>WNT10A</i> , dermatology and dentistry
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Congenital atrichia and hypotrichosis
- Is there a role for dermatologists in eating disorders?
- Inherited Epidermolysis Bullosa: A Clinical Case
- Australasian Society for Dermatology Research Meeting, May 2006
- Dermatological Issues in a Child with Diabetes Mellitus
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Cell-free regenerative medicine: identifying the best source of mesenchymal stem cells for skin therapy in Systemic Sclerosis
- Dermatologic Signs in Patients with Eating Disorders
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- A rare case of woolly hair with unusual associations
- Beyond cancer treatment: dermo-aesthetic and other wellness recommendations for breast cancer patients
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Schimmelpenning Syndrome: A Neuro-Oculo-Cutaneous Disorder
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Acne-Associated Syndromes