Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Chad Johnston"'
Publikováno v:
JAAD Case Reports, Vol 14, Iss , Pp 72-74 (2021)
Externí odkaz:
https://doaj.org/article/d3ab2a4639f04cc4817bca95dfb24c9f
Publikováno v:
JAAD Case Reports, Vol 6, Iss 10, Pp 1029-1031 (2020)
Externí odkaz:
https://doaj.org/article/6a7df02820dd4b4d9ae913aa977646bb
Publikováno v:
JAAD Case Reports, Vol 6, Iss 6, Pp 531-533 (2020)
Externí odkaz:
https://doaj.org/article/cec96a2b6c964302bcfd46ad2597f626
Publikováno v:
HCA Healthc J Med
BACKGROUND: Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a life-threatening, multi-organ adverse drug reaction with an incidence of 1 in 1000 to 1 in 10 000 high-risk drug exposures. CASE PRESENTATION: An elderly female p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2fa0739e743549e4c3d63a1331aba36
https://europepmc.org/articles/PMC10324870/
https://europepmc.org/articles/PMC10324870/
Publikováno v:
HCA Healthc J Med
Description The following case study demonstrates a 26-year-old male that presented to the dermatology clinic with an enlarging, raised skin nodule located on the left inferior lateral lower back. The patient reported it had persisted for two years,
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 6, Iss 6, Pp 531-533 (2020)
JAAD Case Reports, Vol 6, Iss 6, Pp 531-533 (2020)
Publikováno v:
HCA Healthc J Med
Description Simpson-Golabi-Behmel syndrome is a rare, X-linked recessive syndrome associated with mutations in the genes encoding glypican 3 (GPC3). The majority of cases have been described in pediatric males, with those affected showing manifestati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2461d705ce29828dae5c011bf71383e
https://europepmc.org/articles/PMC10324786/
https://europepmc.org/articles/PMC10324786/
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 6, Iss 10, Pp 1029-1031 (2020)
JAAD Case Reports, Vol 6, Iss 10, Pp 1029-1031 (2020)
Publikováno v:
HCA Healthc J Med
INTRODUCTION: Red Ear Syndrome (RES) is a condition often considered to be a localized form of erythromelalgia. It can be related to structural cervical defects or idiopathic. RES is generally very difficult to treat. DISCUSSION: A 57-year-old male p
Autor:
Chad Johnston
This book is a compilation of significant reports and testimonies issued in August 2018.