Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Jennifer L. Hand"'
Autor:
Kuldeep Singh, DO, Olivia M. Crum, MD, Dawn Marie R. Davis, MD, Steven L. Moran, MD, Jennifer L. Hand, MD
Publikováno v:
JAAD Case Reports, Vol 6, Iss 10, Pp 1012-1015 (2020)
Externí odkaz:
https://doaj.org/article/9b64b6805dae42078e25c56ac5b0c3a8
Publikováno v:
Dermatologic Clinics. 41:175-185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b3e51d015570a1c8834e71aeb9a7f0a
https://doi.org/10.1016/j.det.2022.07.013
https://doi.org/10.1016/j.det.2022.07.013
Autor:
Dawn Marie R. Davis, Jennifer L. St. Sauver, Jennifer L. Hand, Megha M. Tollefson, Reese L. Imhof, Amy L. Weaver
Publikováno v:
Journal of the American Academy of Dermatology. 87:409-411
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ace4c4910f965139426083327f39178c
https://doi.org/10.1016/j.jaad.2021.08.030
https://doi.org/10.1016/j.jaad.2021.08.030
Publikováno v:
Dermatologic clinics. 41(1)
Skin cancers represent the most common malignancy worldwide. In children, the diagnosis of skin cancer is rare and raises the possibility of an underlying genetic predisposition. Recent molecular advances have increased understanding of certain genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56be3a0e50df1d3e74dd83c5ed45c494
https://pubmed.ncbi.nlm.nih.gov/36410977
https://pubmed.ncbi.nlm.nih.gov/36410977
Publikováno v:
Pediatric Dermatology. 38:73-78
BACKGROUND/OBJECTIVES Trisomy 21 has known associated clinical phenotypes, including skin and soft tissue concerns. However, the overall prevalence and types of findings are largely unclear. METHODS A retrospective review of children with trisomy 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5357c391095d605a4cad3af2b57661b
https://doi.org/10.1111/pde.14764
https://doi.org/10.1111/pde.14764
Publikováno v:
Pediatric dermatologyREFERENCES. 39(5)
Basal cell nevus syndrome (BCNS) is an autosomal dominant skin cancer predisposition syndrome associated with abnormal mineral metabolism, a risk factor for urinary stone disease (USD). However, no research investigating the association between BCNS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a39bf8e70617b04f5f05d15a569c097
https://pubmed.ncbi.nlm.nih.gov/35574616
https://pubmed.ncbi.nlm.nih.gov/35574616
Autor:
Christine Wassel, Lisa Breuning, Shane M Swink, Jennifer L. Hand, Sarah Asch, Jean R. Pickford, Leslie Castelo-Soccio, Karina L. Vivar, Leonard M. Milstone
Publikováno v:
Pediatric Dermatology. 38:137-142
Background/objectives Patients with rare diseases are challenged when it comes to finding physicians with expertise in their condition. The Foundation for Ichthyosis and Related Skin Types (FIRST) Tele-Ichthyosis program has provided telemedicine for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f6b650e14555b220204c3a4db77c0c
https://doi.org/10.1111/pde.14460
https://doi.org/10.1111/pde.14460
Publikováno v:
Journal of the American Academy of Dermatology. 83:1323-1330
Background Drug reaction with eosinophilia and systemic symptoms (DRESS) is a drug-induced hypersensitivity reaction that can have fatal complications. Although substantial data exist regarding DRESS in adults, to our knowledge, a systematic review o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2356c0d636cd9ba147cda2c36539079f
https://doi.org/10.1016/j.jaad.2020.03.081
https://doi.org/10.1016/j.jaad.2020.03.081
Autor:
Somaira Nowsheen, Jennifer L. Hand, Megha M. Tollefson, Dawn Marie R. Davis, David A. Wetter, Erin Roberts
Publikováno v:
Pediatric Dermatology. 38:72-76
Background/objectives Studies assessing the utility of spironolactone for treating acne in adolescent females are lacking. Thus, we sought to examine spironolactone's role in treating this patient population. Methods A retrospective review was perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::832884078189413a49a49cb9329a3f2d
https://doi.org/10.1111/pde.14391
https://doi.org/10.1111/pde.14391
Autor:
Eric W. Klee, Peter J. Tebben, Cherisse A. Marcou, Lisa A. Schimmenti, Linda Hasadsri, Jennifer L. Hand, Erica L. Macke, Karthik Muthusamy
Publikováno v:
American Journal of Medical Genetics Part A. 182:2442-2449
Prader-Willi syndrome (PWS) is a prototypic genetic condition related to imprinting. Causative mechanisms include paternal 15q11-q13 deletion, maternal chromosome 15 uniparental disomy (UPD15), Prader-Willi Syndrome/Angelman Syndrome (PWS/AS) critica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::921a7d83798f1e6b3e8473573790cc5d
https://doi.org/10.1002/ajmg.a.61792
https://doi.org/10.1002/ajmg.a.61792