Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Madeline Weiner"'
Publikováno v:
Journal of the American Academy of Dermatology. 60:203-211
Background Case series have demonstrated that potentially lethal cutaneous squamous cell carcinomas arise in patients with recessive dystrophic epidermolysis bullosa (RDEB), although the magnitude of this risk is undefined. Methods Systematic case fi
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 46:147-158
Background Portions of the gastrointestinal (GI) tract may be severely involved in patients with inherited epidermolysis bullosa (EB). Evidence-based data are lacking as to the frequency and time of onset of these complications. Patients and methods
Publikováno v:
The British Journal of Dermatology
Background Case reports have suggested that cardiomyopathy may be a complication of recessive dystrophic epidermolysis bullosa (RDEB). Objective To determine the risk of congestive heart failure (CHF) or cardiomyopathy in each major EB subtype. Metho
Autor:
Madeline Weiner, Anne W. Lucky, Francis Palisson, Elizabeth I. Pillay, Anna L. Bruckner, Jemima E. Mellerio, Jacqueline E. Denyer
Publikováno v:
International Journal of Dermatology. 46:795-800
Autor:
Elizabeth I. Pillay, Ellen Pfendner, Judy Paskel, Francis Palisson, Anne W. Lucky, Madeline Weiner
Publikováno v:
International Journal of Dermatology. 46:809-814
Autor:
David T. Devries, Joy DeLeoz, Sarah Cash, Amy Stein, Madeline Weiner, Chirayath M. Suchindran, Jo-David Fine, Lorraine Johnson
Publikováno v:
Journal of Urology. 172:2040-2044
We determined the frequency with which 6 genitourinary tract complications (urethral meatal stenosis, urinary retention, bladder hypertrophy, hydronephrosis secondary to ureteral strictures, pyelonephritis and cystitis) occur in inherited epidermolys
Autor:
Jo-David, Fine, Lorraine B, Johnson, Madeline, Weiner, Amy, Stein, Sarah, Cash, Joy, DeLeoz, David T, Devries, Chirayath, Suchindran
Publikováno v:
American Journal of Kidney Diseases. 44:651-660
Isolated case reports and limited clinical series suggested that renal failure may occur in some patients with inherited epidermolysis bullosa (EB). Reported causes have included poststreptococcal glomerulonephritis, secondary amyloidosis, and chroni
Publikováno v:
Journal of the American Academy of Dermatology. 50:572-581
Background Inherited epidermolysis bullosa (EB) encompasses 4 major types and at least 23 clinically distinctive phenotypes. Although considerable variability in cutaneous disease activity is known to exist within each, severity and anatomic distribu
Autor:
Jack, Twersky, Terry, Montgomery, Richard, Sloane, Madeline, Weiner, Susan, Doyle, Kavita, Mathur, Mary, Francis, Kenneth, Schmader
Publikováno v:
Ostomy/wound management. 58(12)
Pressure ulcer prevention is an important aspect of nursing home care. A 20-week, unblinded, randomized, controlled trial was conducted to compare the rate of nursing home-acquired pressure ulcers and adverse events between residents managed using: 1
Autor:
T. Conrad Gilliam, Jo-David Fine, Jurg Ott, Madeline Weiner, Jianjun Liu, Amalia Martinez-Mir, Wasim Ahmad, Derek Gordon, Angela M. Christiano
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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8 páginas, 1 figura, 1 tabla.
Epidermolysis bullosa simplex (EBS) is an inherited blistering disease characterized by intraepidermal cleavage (Gedde-Dahl and Anton-Lamprecht, 1990;Fine et al, 1991). A very rare subset of EBS, termed "EBS superf
Epidermolysis bullosa simplex (EBS) is an inherited blistering disease characterized by intraepidermal cleavage (Gedde-Dahl and Anton-Lamprecht, 1990;Fine et al, 1991). A very rare subset of EBS, termed "EBS superf