![]() | WILLIAM L WestonEmeritus Professor, Departments of Dermatology and Pediatrics,The Children's Hospital and University of Colorado Hospital, Denver, Colorado, Estados Unidos | Emeritus ... |
KOL Resume for WILLIAM L Weston
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2008 | Emeritus Professor, Departments of Dermatology and Pediatrics,The Children's Hospital and University of Colorado Hospital, Denver, Colorado, Estados Unidos |
2007 | Emeritus Professor, Departments of Dermatology and Pediatrics, The Children's Hospital and University of Colorado Hospital, Denver, Colorado, USA |
2006 | Department of Dermatology, University of Colorado at Denver and Health Sciences Center, Aurora, Colorado, USA |
2005 | Department of Dermatology, University of Colorado Health Sciences Center, Aurora, CO University of Colorado School of Medicine, Denver, USA. |
2004 | Pediatrics, University of Colorado Health Sciences Center, Denver, Colorado, and ‡Division of Dermatology, University of Alberta, Edmonton, Alberta, Canada Department of Dermatology, University of Colorado Health Sciences Center, Aurora, Colorado |
2003 | Departments of Pediatrics and Dermatology, University of Colorado Health Sciences Center, Denver, Colorado, and |
2002 | Department of Dermatology, University of Colorado Health Sciences Center, Denver, Colorado, |
2001 | Department of Dermatology, University of Colorado Health Science Center, Denver, Colorado |
2000 | Department of Rheumatology and Medicine, Hospital for Joint Diseases, New York University School of Medicine, New York, New York; Departments of Dermatology, Medicine, and Pediatrics, University of Colorado Health Sciences Center, Denver; and Dermatology Service, Department of Medicine, Denver Health Medical Center, Colorado Denver, Colo |
1999 | Department of Dermatology, University of Colorado School of Medicine, Denver, Colorado |
1998 | Department of Dermatology, University of Colorado Health Sciences Center. Denver, Colorado |
1997 | University of Colorado Health Sciences Center, Department of Denver, Colorado, U.S.A. From the Department of Dermatology,a the Departments of Dermatology and Pediatrics,b and Royal Alexandria Hospital for Children.c Denver, Colorado, and Sydney, Australia |
1996 | From the Department of Dermatology, University of Colorado School of Medicine, Denver, Colorado Denver, CO |
1995 | Departments of Dermatology and Pediatrics, University of Colorado School of Medicine, Denver, CO 80262 Department of Dermatology, University of Colorado Denver, Colorado, USA. |
1994 | University of Colorado Health Sciences Center, Department of Dermatology, Denver, CO 80262 U.S.A. |
1993 | Department of Dermatology, University of Colorado Health Sciences Center, Denver, Colorado, U.S.A. Denver, Colorado, USA Pediatric Dermatology Fellow, University of Colorado School of Medicine, Denver |
1992 | Department of Pediatrics, University of Colorado Health Sciences Center, Denver, Colorado 80262 Professor of Dermatology and Pediatrics University of Colorado School of Medicine Denver, Colorado, USA Dermatology Service of the Veterans Affairs Medical Center, Denver, Colorado, U.S.A. |
1991 | Rochester, New York, USA |
1990 | Department of Dermatology University of Colorado School of Medicine Denver, Colorado, USA |
1989 | Department of Dermatology, University of Colorado Medical School, Denver, Colorado |
1988 | Department of Dermatology, Pharmacology, and Pediatrics, University of Colorado School of Medicine, Denver, Colorado, U.S.A. |
1987 | U. of Colorado Medical Center, Denver, Colorado |
1986 | Division of Dermatology, Department of Medicine, University of Utah School of Medicine, Salt Lake City Department of Surgery, University of California at San Diego, San Diego, California, U.S.A. Denver, CO, USA |
1985 | Departments of Dermatology and Internal Medicine, University of Colorado Medical School, Denver, Colorado, U.S.A. Department of Dermatology, University of Colorado School of Medicine, Denver Columbus, OH, USA |
1984 | From the Department of Dermatology, University of Colorado School of Medicine Department of Dermatology, University of Colorado Health Sciences Center, Denver, Colorado 80262 USA |
1983 | Department of Dermatology, University of Colorado School of Medicine, Boulder, Colorado Scripps Institute, La Jolla, Calif. USA |
1982 | From the Department of Dermatology, University of Colorado Medical Center. University of Colorado School of Medicine, Denver, Colorado, U.S.A. |
1981 | From the Department of Dermatology, the Divisions of Rheumatic Diseases and Clinical Immunology of the Department of Medicine, and the Departments of Ophthalmology and Pediatrics, University of Colorado Health Sciences Center, Denver, CO, USA Departments of Dermatology, Paediatrics and Internal Medicine, University of Colorado Health Sciences Center, Denver, Colorado, U.S.A |
1980 | Departments of Pediatrics and Dermatology, University of Colorado Health Sciences Center and the State Home and Training School, Wheatridge, Colorado, U.S.A. Department of Medicine, National Jewish Hospital, Denver, Colorado |
WILLIAM L Weston: Influence Statistics
Concept | World rank |
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children antibodymediated allergies | #1 |
vacciniforme keratitis | #1 |
humoral monocyte | #1 |
ssaro sera | #1 |
defective migration vivo | #1 |
fortyone control subjects | #1 |
monocytemacrophage function | #1 |
inhibition cryoimmunoglobulin | #1 |
unusual presentation dh | #1 |
orange acyclovir | #1 |
normal phagocytosis opsonisation | #1 |
17 neonatal lupus | #1 |
phagocytic syndrome | #1 |
wbc count pustules | #1 |
7 melanoma patients | #1 |
granuloma children | #1 |
boys severe necrosis | #1 |
multiforme female | #1 |
aphthous viremia rau | #1 |
diluted conjugated antisera | #1 |
syndrome erythema | #1 |
institutionalised individuals | #1 |
swab peripheral | #1 |
multiforme acute | #1 |
incubation chamber background | #1 |
multiforme adolescent | #1 |
differences neutrophil phagocytosis | #1 |
treatment ulcerated | #1 |
cutaneous male pedigree | #1 |
fourteen individuals syndrome | #1 |
improvement chemotaxis | #1 |
cutaneous mastocytosis diffuse | #1 |
herpetiformis presenting | #1 |
nle crusted | #1 |
herpesassociated | #1 |
rau acute | #1 |
study hladr synthesis | #1 |
neonatal tinea capitis | #1 |
chemotaxis bcg | #1 |
pyogenic granuloma children | #1 |
hladr expression hk | #1 |
c1q skin | #1 |
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Prominent publications by WILLIAM L Weston
In this study we examined the rate of decrease in size of facial port wine stains (PWS) as a function of number of treatments, lesion size, lesion location and patients' age. This study was performed at the University of Colorado Hospital Outpatient Dermatology Center, Denver, U.S.A. A consecutive sample of 91 patients 18 years of age or younger with facial PWS in which the entire lesion was treated at each visit were studied. Included were all patients who had a minimum of five ...
Known for Pulsed Dye | Port Wine | 585 Nm | Pws Patients | Lesion Size |
The association between erythema multiforme (EM) and herpes simplex virus (HSV) infection has long been appreciated, although the exact role which HSV may play in the pathogenesis of this herpes-associated EM (HAEM), is unknown. Previous studies have suggested, but not definitively demonstrated, the presence of HSV in lesions of HAEM. The presence of HSV would support the hypothesis that an immune-mediated response directed against HSV-specific antigens in the skin is central to lesion ...
Known for Cutaneous Lesions | Herpes Simplex | Hsv Dna | Situ Hybridization | Erythema Multiforme |
Detection of herpes simplex virus DNA in the peripheral blood during acute recurrent herpes labialis
[ PUBLICATION ]
BACKGROUND: Although herpes simplex virus (HSV) has been detected in the peripheral blood of immunocompromised patients and in neonates with disseminated disease, the extent to which this virus may be present in the blood during a localized infection in otherwise healthy adults is unknown.
OBJECTIVE: The purpose of this study was to determine whether HSV may be detected in the peripheral blood during acute recurrent herpes labialis.
METHODS: Peripheral blood mononuclear cells (PBMCs) ...
Known for Peripheral Blood | Herpes Simplex Virus | Hsv Dna | Acute Episode | Disseminated Disease |
OBJECTIVES: The present study describes the demographics, mortality, morbidity and recurrence rates of autoimmune-associated congenital heart block (CHB) using information from the Research Registry for Neonatal Lupus.
BACKGROUND: Isolated CHB detected at or before birth is strongly associated with maternal autoantibodies to 48-kD SSB/La, 52-kD SSA/Ro and 60-kD SSA/Ro ribonucleoproteins and is a permanent manifestation of the neonatal lupus syndromes (NLS). Available data are limited by ...
Known for Recurrence Rate | Neonatal Lupus | Heart Block | Mortality Morbidity | Subsequent Pregnancies |
Human keratinocytes produce biologically active pro-IL-1 alpha and inactive pro-IL-1 beta with most protein remaining intracellular. IL-1 receptor antagonist (IL-1ra) is a newly described member of the IL-1 family that is secreted by stimulated monocytes and binds competitively to IL-1 receptors without stimulating target cells. We examined the characteristics of IL-1ra production by cultured human keratinocytes. By ELISA, keratinocyte lysates contained 390 ng IL-1ra/mg total protein ...
Known for Human Keratinocytes | Il1ra Il1 | Receptor Antagonist | Protein Interleukin1 | Western Blot Analysis |
Ultraviolet light induces binding of antibodies to selected nuclear antigens on cultured human keratinocytes.
[ PUBLICATION ]
Antibodies which bind to different nuclear antigens in tissue sections or in permeabilized cell cultures are useful markers of subsets of connective tissue disease, especially of lupus erythematosus (LE), but whether these antibodies are able to react with these intracellular sequestered antigens in vivo and cause immunologic tissue damage has been a matter of much debate. We report experiments which show that ultraviolet light-irradiated, cultured human keratinocytes bind IgG antibodies ...
Known for Nuclear Antigens | Ultraviolet Light | Human Keratinocytes | Cell Surface | Dna Anti |
Cutaneous manifestations of neonatal lupus without heart block: Characteristics of mothers and children enrolled in a national registry
[ PUBLICATION ]
OBJECTIVE: To extend the information base on cutaneous manifestations of neonatal lupus erythematosus (NLE) with regard to maternal disease, sex of child, onset, localization, influence of UV light, prognosis, and recurrence rates in subsequent pregnancies.
METHODS: Review of records from the Research Registry for Neonatal Lupus.
RESULTS: The cohort includes 47 mothers (83% white) whose sera contain anti-SSA/Ro, anti-SSB/La, and/or anti-U1-ribonucleoprotein antibodies and their 57 ...
Known for Heart Block | Cutaneous Manifestations | Neonatal Lupus | National Registry | Subsequent Pregnancies |
OBJECTIVE: To investigate our hypothesis that recurrent aphthous stomatitis (RAS), an inflammatory disease of the oral mucosa, is the result of an abnormal oral mucosal cytokine cascade leading to an enhanced cell-mediated immune response directed toward focal areas of the oral mucosa.
DESIGN: Prospective nonrandomized case-control study.
SETTING: Academic referral center
PATIENTS: For part 1, 21 patients with RAS and 7 control patients; for part 2, 6 patients with RAS and 6 control ...
Known for Oral Mucosa | Tumor Necrosis | Interferon Gamma | Aphthous Stomatitis | Patients Ras |
Langerhans cell histiocytosis (LCH) is a disease characterized by Langerhans cell infiltration of skin and bone, with its most severe form manifested by multifocal infiltration of many organs. The etiology is unknown, although viral infection has been proposed as a potential pathogenic factor. Human herpesvirus 6 (HHV-6), a recently described member of the human herpesvirus family, has been associated with atypical or malignant lymphocytic processes, and immune disorders. Based on these ...
Known for Human Herpesvirus | Langerhans Cell | Hhv6 Dna | Lch Disease | 30 Patients |
Examination of cutaneous T‐cell lymphoma for human herpesviruses by using the polymerase chain reaction
[ PUBLICATION ]
The etiology of cutaneous T-cell lymphoma remains unknown, although an association with viral infection, in particular certain retroviruses and human herpesviruses, has been suggested. The purpose of this study was to examine skin biopsies of cutaneous T-cell lymphoma for the presence of Epstein-Barr virus, herpes simplex virus type 1 and type 2, and human herpesvirus-6 by using the polymerase chain reaction. Lesional skin biopsies from 30 patients with cutaneous T-cell lymphoma were ...
Known for Human Herpesvirus | Polymerase Chain Reaction | Cell Lymphoma | Epsteinbarr Virus | Skin Biopsies |
OBJECTIVE: To evaluate the response of facial port-wine stains in children to pulsed (450 microseconds) dye (577- or 585-nm) laser treatment based on the age of the patient and the size of the port-wine stain at the initiation of treatments.
DESIGN: Case series.
SETTING: Outpatient dermatology clinic at the University of Colorado School of Medicine, Denver.
PATIENTS: A consecutive sample of 83 children who had facial port-wine stains that were treated in their entirety at each ...
Known for Wine Stains | Dye Laser | Patients Port | Complete Clearing | Lesion Size |
The association between infection with HSV and the subsequent development of erythema multiforme is well established, although the role that the virus plays in the pathogenesis of this disorder is not known. HSV DNA has been detected in cutaneous lesions of herpes-associated erythema multiforme (HAEM), and it has been suggested that the tissue damage seen in these lesions is virus-specific. In the current, prospective study, we examined biopsies of lesional, non-involved, and previously ...
Known for Erythema Multiforme | Hsv Dna | Simplex Virus | Peripheral Blood | Skin Patients |
Treatment of Pyogenic Granuloma in Children With the Flashlamp-pumped Pulsed Dye Laser
[ PUBLICATION ]
OBJECTIVE: Pyogenic granuloma is a common, acquired, vascular tumor of the skin in children, often ulcerates or bleeds, and is commonly localized to the face. The treatment of choice has been surgical removal, either by excision or shave, followed by electrocautery. The site, young age of the patient, and the inherent nature of surgical removal or electrocautery often make this procedure a traumatic experience. Also, surgical treatment usually leads to permanent scarring. Owing to the ...
Known for Pyogenic Granuloma | Dye Laser | Skin Lesions | 20 Patients | 2 Weeks |
Key People For Erythema Multiforme
WILLIAM L Weston:Expert Impact
Concepts for whichWILLIAM L Westonhas direct influence:Erythema multiforme, Lupus erythematosus, Atopic dermatitis, Monocyte chemotaxis, Neonatal lupus, Oral mucosa, Human herpesvirus, Dermatitis herpetiformis.
WILLIAM L Weston:KOL impact
Concepts related to the work of other authors for whichfor which WILLIAM L Weston has influence:Lupus erythematosus, Erythema multiforme, Atopic dermatitis, Heart block, Tissue factor, Mycosis fungoides, Topical corticosteroids.
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