Professor, Dermatology, UCSF School of Medicine

Dermatology

Bruce Wintroub practices Dermatology. He attended Washington University School of Medicine in St. Louis. He received 3 awards: "CMS Meaningful Use Stage 1 Certification", "Elected Member" and "Whos Who in Medicine and Healthcare". Dr. Bruce U. Wintroub is also published. He has 64 publications published. The lastest publication: "Cyclosporine as maintenance therapy in patients with severe psoriasis.' He accepts all Medicare patients.

Publications

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• Increasing racial and ethnic diversity in dermatology: A call to action.
• Treatment of cutaneous T-Cell lymphoma by extracorporeal photochemotherapy. Preliminary results.
• Cyclosporine as maintenance therapy in patients with severe Psoriasis.
• Treatment of systemic sclerosis with extracorporeal photochemotherapy. Results of a multicenter trial.
• Treatment of erythrodermic cutaneous T-Cell lymphoma with extracorporeal photochemotherapy.
• Identification of a cathepsin G-like proteinase in the MCTC type of human mast Cell.
• The evolution of Lesions in erythema elevatum diutinum.
• A systematic review of the safety of topical therapies for Atopic dermatitis.
• Dermatology, the academic medical center, and the new millennium.
• The molecular pathogenesis of bullous Pemphigoid.
• Serial subculture and relative transport of human endothelial Cells in serum-free, defined conditions.
• Human mast Cell carboxypeptidase.
• Human mast Cell carboxypeptidase. Selective localization to MCTC Cells.
• Human skin mast Cell carboxypeptidase: functional characterization, cDNA cloning, and genealogy.
• A pilot study of piritrexim in mycosis fungoides.
• A phagocytosis-enhancing factor in human plasma.
• A neutrophil-dependent pathway for the generation of a neutral peptide mediator. II. SubCellular localization of the neutrophil protease.
• Identification of chemoattractant activity for lymphocytes in bullous Pemphigoid bullous fluid.
• Morphologic and functional evidence for release of mast-Cell products in bullous pemphigoid.
• Purification and characterization of a human neutrophil neutral protease. The neutral peptide-generating protease.
• The impact of managed care on graduate medical education and academic medical centers.
• The preferential human mononuclear leukocyte chemotactic activity of the substituent tetrapeptides of angiotensin II.
• Bullous pemphigoid, an ultrastructural study of the inflammatory response: eosinophil, basophil and mast Cell granule changes in multiple biopsies from one patient.
• Mast Cell-dependent effector pathways and cutaneous bullous disorders.
• Biology of the mast Cell and its role in cutaneous inflammation.
• A human neutrophil-dependent pathway for generation of angiotensin II. Purification of the product and identification as angiotensin II.
• Cleavage of fibrinogen by the human neutrophil neutral peptide-generating protease.
• Dermatologic training for nondermatologists.
• Dermatologic practice: implications for a primary care residency curriculum.
• A human neutrophil-dependent pathway for generation of angiotensin II: purification and physicochemical characterization of the plasma protein substrate.
• Disseminated cryptococcosis presenting as herpetiform Lesions in a homosexual man with acquired immunodeficiency syndrome.
• Granulocyte-angiotensin system. Identification of angiotensinogen as the plasma protein substrate of leukocyte cathepsin G.
• Lymphocyte subsets and Langerhans Cells/indeterminate Cells in erythema multiforme.
• Identification of chemoattractant activity for lymphocytes in blister fluid of patients with bullous Pemphigoid: evidence for the presence of a lymphokine.
• Erythema multiforme: microvascular damage and infiltration of lymphocytes and basophils.
• The granulocyte-angiotensin system. Angiotensin I-converting activity of cathepsin G.
• Separation of angiotensins and assay of angiotensin-generating enzymes by high-performance liquid chromatography.
• Identification of a human neutrophil angiotension II-generating protease as cathepsin G.
• Inflammation and mediators.
• Angiotensin I conversion by human and rat chymotryptic proteinases.
• Hemodynamic response to dopamine in experimental myocardial infarction.
• The pulmonary and systemic circulatory response to dopamine infusion.
• A neutrophil-dependent pathway for the generation of a neutral peptide mediator: partial characterization of components and control by alpha-1-antitrypsin.
• Lamellar body-enriched fractions from neonatal mice: preparative techniques and partial characterization.
• Pott's puffy tumor. A clinical marker for osteomyelitis of the skull.
• Selective expression of 15-lipoxygenase activity by cultured human keratinocytes.
• Photosensitivity due to drugs.
• A human lung mast Cell chymotrypsin-like enzyme. Identification and partial characterization.
• Human neutrophils release serine proteases capable of activating prorenin.
• The fibrinogenolytic activity of purified tryptase from human lung mast Cells.
• Inhibition of angiotensin-converting enzyme by des-Leu10-angiotensin I: a potential mechanism of endogenous angiotensin-converting enzyme regulation.
• A human platelet angiotensin I-processing system. Identification of components and inhibition of angiotensin-converting enzyme by product.
• Chemistry of a human monocyte-derived Cell line (U937): identification of the angiotensin I-converting activity as leukocyte cathepsin G.
• Adverse drug reactions: reporting and evaluating cutaneous reactions.
• Drug reactions.
• Cutaneous drug reactions: pathogenesis and clinical classification.
• Human mast Cell carboxypeptidase. Purification and characterization.
• Mast Cell carboxypeptidase: biochemistry and biology.
• Combined total body X-ray irradiation and total Skin electron beam radiotherapy with an improved technique for mycosis fungoides.
• Mast Cell and eosinophil mediated damage in bullous pemphigoid.
• In vitro pemphigus vulgaris model using organotypic cultures of human epidermal keratinocytes.
• Erythropoietin binding and induced differentiation of Rauscher erythroleukemia Cell line red 5-1.5.
• Detection and partial characterization of a human mast Cell carboxypeptidase.

Schools

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• Washington University St Louis

• Peter B Brigham Hospital

• Harvard Med School

• Robert Brigham Hospital

Procedures Preformed

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• Destruction of Benign Skin Lesion
• Excision of Malignant Skin Lesion
• Shaving of Skin Lesion

Conditions Treated

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• Acne
• Actinic Keratosis
• Athlete's Foot
• Atopic Dermatitis (Eczema)
• View All

Doctors Specialties

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• Dermatology
• Internal Medicine

Accepted Insurances

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Awards

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• CMS Meaningful Use Stage 1 Certification
• Elected Member
• Whos Who in Medicine and Healthcare

Education

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• Massachusetts General Hospital
• Brigham and Women's Hospital
• Washington University School of Medicine in St. Louis

Hospital

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• San Francisco General Hospital and Trauma Center
• UCSF Medical Center

Drug Facts

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NPI NUMBER		1487604286
NPPES Provider LastName		WINTROUB
NPPES Provider FirstName		BRUCE
NPPES Provider ZIPCode		941153011
NPPES Provider State		CA
Specialty Description		Dermatology
Total Claim Count		123.0
Distinct Opioid Count		0.0
Opioid Claim Count		0.0
Percent Opioid Claims		0.0

Helpful Reviews

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Medicare Facts

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National Provider Identifier [NPI]	1487604286
Last Name Of The Provider	WINTROUB
First Name Of The Provider	BRUCE
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