A5036748801- Cutaneous lymphoproliferative disorders research
- Lymphoma Diagnosis and Treatment
- Sleep and Wakefulness Research
- Cutaneous Melanoma Detection and Management
- Fungal Infections and Studies
- Acute Myeloid Leukemia Research
- Vascular Tumors and Angiosarcomas
- Sleep and related disorders
- Autoimmune Bullous Skin Diseases
- Nonmelanoma Skin Cancer Studies
- Chronic Lymphocytic Leukemia Research
- Neuroscience of respiration and sleep
- T-cell and Retrovirus Studies
- CAR-T cell therapy research
- Artificial Intelligence in Healthcare and Education
- Obstructive Sleep Apnea Research
- Chemotherapy-related skin toxicity
- Histone Deacetylase Inhibitors Research
- Impact of AI and Big Data on Business and Society
- Antimicrobial Resistance in Staphylococcus
- Inflammatory Myopathies and Dermatomyositis
- AI in cancer detection
- Immunodeficiency and Autoimmune Disorders
- Urticaria and Related Conditions
- Hair Growth and Disorders
New York University
2021-2024
Yale University
2015-2021
NYU Langone Health
2019
National Heart Lung and Blood Institute
2012
National Institutes of Health
2012
High-throughput sequencing of T cell receptors to define and quantify populations emerges as a diagnostic tool with the remarkable ability discriminate between CTCL benign inflammatory conditions (Kirsch et al., this issue).
Abstract Bullous systemic lupus erythematosus ( BSLE ) is a rare subepidermal blistering disorder characterized by an acute vesiculobullous eruption in subset of individuals with erythematosus. most commonly affects young women and only rarely children. Herein we report case 6‐year‐old boy.
YL (Junior Doctor): A 36-year-old man was observed by his wife to have irregular breathing with sighs followed recurrent episodes of prolonged cessation while falling asleep. The longest witnessed pause lasted approximately 3 min and during this time lips became cyanotic. patient unaware these until informed him. No wheezing, stridor, cough, gurgle or vomiting episodes. detailed interview revealed that the had a history obstructive sleep apnoea inferior turbinate hypertrophy undergone an...
Graham-Little-Piccardi-Lasseur syndrome is a rare dermatosis that affects the hair follicles throughout body and often presents with progressive cicatricial alopecia of scalp unresponsive to medical therapy.While treatment options are limited, prompt recognition through careful physical exam aided by dermoscopy can facilitate early intervention.Here we present patient GLPLS, discuss pertinent morphologic dermoscopic findings, review current literature.
The erythrodermic patient is often challenging and requires careful evaluation. Work-up should include an extensive medication history, histological laboratory testing, if necessary, molecular studies for the evaluation of underlying malignancy. Herein, we present with repeated biopsies demonstrating a spongiotic process who was found to have circulating atypical T-cells concerning T-cell leukemia, most closely related Sézary syndrome.