Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lauren Banner"'
Autor:
Daniel Joffe, BS, Thomas Z. Rohan, BS, Jenna Mandel, BS, Jayson Suriano, BA, Lauren Banner, BS, Alexander Valiga, MD, Pierluigi Porcu, MD, Jerald Z. Gong, MD, Jason B. Lee, MD, Onder Alpdogan, MD, Neda Nikbakht, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 49, Iss , Pp 51-54 (2024)
Externí odkaz:
https://doaj.org/article/67d7f782c7e74d26866eaa0c598deea1
Autor:
Safiyyah Bhatti, Daniel Joffe, Lauren Banner, Sahithi Talasila, Jenna Mandel, Jason Lee, Pierluigi Porcu, Neda Nikbakht
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Cutaneous adverse events of both topical and systemic drugs in patients with mycosis fungoides (MF) present a diagnostic challenge as it is often difficult to distinguish drug associated rash from disease progression in the skin. Mogamulizumab and me
Externí odkaz:
https://doaj.org/article/21b65495e0024c6891d8f2b0112e3f47
Autor:
Laura Gleason, Daniel Joffe, Safiyyah Bhatti, Alexa Cohen, Lauren Banner, Emily Correia, Onder Alpdogan, Pierluigi Porcu, Neda Nikbakht
Publikováno v:
Case Reports in Oncology, Vol 15, Iss 3, Pp 1088-1094 (2022)
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare subtype of cutaneous T-cell lymphoma that usually presents with tender subcutaneous nodules on the trunk and extremities. Immunosuppressive therapy is considered first-line treatment fo
Externí odkaz:
https://doaj.org/article/64fee2230e8644f1afdd9432c91a0d71
Publikováno v:
Dermatology Practical & Conceptual, Vol 13, Iss 3 (2023)
Introduction: Lymphedema often presents as progressive, unremitting swelling and skin changes that are extremely distressing to patients. Hereditary lymphedema (HL) constitutes a type of primary lymphedema that is passed down through generations. Obj
Externí odkaz:
https://doaj.org/article/b9d3f8c26df044d3bb3ee70d9e48f1ef
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionThe increased incidence of cutaneous melanoma (CM) and Merkel cell carcinoma (MCC) in patients with hematologic malignancies (HM) is well established. While the risk of CM has been assessed in some subtypes of HM including cutaneous T-cel
Externí odkaz:
https://doaj.org/article/4f9f2b6ecfe444b0993eda58780a4848
Autor:
Irfan Chhipa, Zachary Wells, Charles Leinberry, Surena Namdari, Michael Gutman, Lauren Banner
Publikováno v:
Indian Journal of Orthopaedics Surgery. 9:8-11
Lateral elbow tendinopathy is a common condition affecting two to three percent of the population. While non-operative management is the mainstay of treatment, 10-15% remain refractory. Ultrasonic percutaneous tenotomy is a recent therapeutic option
Publikováno v:
Clinical and Experimental Dermatology. 48:431-433
We describe a novel homozygous KRT14 (also known as K14) mutation detected in a patient with a relatively mild form of epidermolysis bullosa simplex (EBS). Our patient harbours loss of function of both alleles of the KRT14 gene. This is the 16th repo