Found: 35
Select item for more details and to access through your institution.
Acral Peeling Skin Syndrome: A Clinically and Genetically Heterogeneous Disorder.
- Published in:
- Pediatric Dermatology, 2012, v. 29, n. 3, p. 258, doi. 10.1111/j.1525-1470.2011.01563.x
- By:
- Publication type:
- Article
Intractable erythematous plaques on the hands: palmoplantar eosinophilic pustular folliculitis.
- Published in:
- International Journal of Dermatology, 2013, v. 52, n. 10, p. 1274, doi. 10.1111/j.1365-4632.2011.05139.x
- By:
- Publication type:
- Article
Thioflavin T as a fluorescence probe for monitoring RNA metabolism at molecular and cellular levels.
- Published in:
- Nucleic Acids Research, 2015, v. 43, n. 14, p. 1, doi. 10.1093/nar/gkv338
- By:
- Publication type:
- Article
Localized Cutaneous Amyloidosis Associated with Poikilodermatous Mycosis Fungoides.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
An Erythematous Plaque on the Breast: A Quiz.
- Published in:
- Acta Dermato-Venereologica, 2013, v. 93, n. 6, p. 763, doi. 10.2340/00015555-1527
- By:
- Publication type:
- Article
Lichen Planus in Childhood Showing Various Cutaneous Features.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
Erythema Annulare Centrifugum-like Neutrophilic Dermatosis: Effects of Potassium Iodide.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
Recurrence of Hydroxyurea-induced Leg Ulcer After Discontinuation of Treatment.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Large Subcutaneous Abscesses Caused by Mycobacterium fortuitum Infection.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Multitasking of Hsp70 chaperone in the biogenesis of bacterial functional amyloids.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0056-0
- By:
- Publication type:
- Article
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 1, p. 26, doi. 10.1038/ejhg.2009.135
- By:
- Publication type:
- Article
Case of hereditary leiomyomatosis and renal cell cancer showing multiple cutaneous leiomyomas harboring a recurrent nonsense mutation in the fumarate hydratase gene.
- Published in:
- Journal of Dermatology, 2022, v. 49, n. 1, p. e42, doi. 10.1111/1346-8138.16223
- By:
- Publication type:
- Article
Severe subcutaneous hematoma in a patient with psoriatic arthritis: Changes of platelet count in psoriatic patients with biologic agents.
- Published in:
- Journal of Dermatology, 2017, v. 44, n. 12, p. 1385, doi. 10.1111/1346-8138.13981
- By:
- Publication type:
- Article
Disappearing subcutaneous papules and nodules: Characteristic features of muscle herniation and piezogenic pedal papules.
- Published in:
- Journal of Dermatology, 2017, v. 44, n. 12, p. e361, doi. 10.1111/1346-8138.14005
- By:
- Publication type:
- Article
Deep venous thrombosis in patients with Behçet's disease.
- Published in:
- Journal of Dermatology, 2015, v. 42, n. 1, p. 101, doi. 10.1111/1346-8138.12741
- By:
- Publication type:
- Article
Pseudolymphoma on the face involving the conjunctiva.
- Published in:
- Clinical & Experimental Dermatology, 2024, v. 49, n. 5, p. 521, doi. 10.1093/ced/llad459
- By:
- Publication type:
- Article
SEMICLASSICAL ORIGIN OF SHELL STRUCTURES IN DEFORMED NUCLEI:: DEPENDENCE ON SURFACE DIFFUSENESS AND EFFECT OF SPIN-ORBIT COUPLINGS.
- Published in:
- International Journal of Modern Physics E: Nuclear Physics, 2004, v. 13, n. 1, p. 191, doi. 10.1142/S0218301304001941
- By:
- Publication type:
- Article
Mild Heat Stress Affects on the Cell Wall Structure in Candida albicans Biofilm.
- Published in:
- Medical Mycology Journal, 2019, v. 60, n. 2, p. 29, doi. 10.3314/mmj.19-00001
- By:
- Publication type:
- Article
Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplex.
- Published in:
- Human Mutation, 2010, v. 31, n. 10, p. E1687, doi. 10.1002/humu.21330
- By:
- Publication type:
- Article
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA<sub>1</sub>α in autosomal recessive hypotrichosis.
- Published in:
- Human Mutation, 2010, v. 31, n. 5, p. 602, doi. 10.1002/humu.21235
- By:
- Publication type:
- Article
Airway stenting in Japan.
- Published in:
- Respirology, 1998, v. 3, n. 4, p. 229, doi. 10.1111/j.1440-1843.1998.tb00127.x
- By:
- Publication type:
- Article
Identification of a Novel Alternatively Spliced Form of Inflammatory Regulator SWAP-70-Like Adapter of T Cells.
- Published in:
- International Journal of Inflammation, 2017, p. 1, doi. 10.1155/2017/1324735
- By:
- Publication type:
- Article
A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testing.
- Published in:
- Experimental Dermatology, 2011, v. 20, n. 1, p. 74, doi. 10.1111/j.1600-0625.2010.01177.x
- By:
- Publication type:
- Article
Erythrokeratoderma Variabilis without Connexin 31 or Connexin 30.3 Gene Mutation: Immunohistological, Ultrastructural and Genetic Studies.
- Published in:
- Acta Dermato-Venereologica, 2003, v. 83, n. 4, p. 266, doi. 10.1080/00015550310016517
- By:
- Publication type:
- Article
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Imaging of bacterial multicellular behaviour in biofilms in liquid by atmospheric scanning electron microscopy.
- Published in:
- Scientific Reports, 2016, p. 25889, doi. 10.1038/srep25889
- By:
- Publication type:
- Article
Complete Paternal Isodisomy of Chromosome 17 in Junctional Epidermolysis Bullosa with Pyloric Atresia.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Genetic Diseases of Junctions.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 12, p. 2713, doi. 10.1038/sj.jid.5700727
- By:
- Publication type:
- Article
Human Bullous Pemphigoid Antigen 2 Transgenic Skin Elicits Specific IgG in Wild-Type Mice.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 12, p. 2807, doi. 10.1038/sj.jid.5700970
- By:
- Publication type:
- Article
Novel ABCA12 Mutations Identified in Two Cases of Non-Bullous Congenital Ichthyosiform Erythroderma Associated with Multiple Skin Malignant Neoplasia.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Patients with Recessive Dystrophic Epidermolysis Bullosa Develop Squamous-Cell Carcinoma Regardless of Type VII Collagen Expression.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 10, p. 2438, doi. 10.1038/sj.jid.5700878
- By:
- Publication type:
- Article
Five New Homozygous Mutations in the KIND1 Gene in Kindler Syndrome.
- Published in:
- 2007
- By:
- Publication type:
- Letter
A Novel GJB2 Mutation p.Asn54His in a Patient with Palmoplantar Keratoderma, Sensorineural Hearing Loss and Knuckle Pads.
- Published in:
- 2007
- By:
- Publication type:
- Letter
The South African “Bathing Suit Ichthyosis” Is a Form of Lamellar Ichthyosis Caused by a Homozygous Missense Mutation, p.R315L, in Transglutaminase 1.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Changing Pattern of Deiminated Proteins in Developing Human Epidermis.
- Published in:
- Journal of Investigative Dermatology, 2003, v. 120, n. 5, p. 817, doi. 10.1046/j.1523-1747.2003.12138.x
- By:
- Publication type:
- Article