Zobrazeno 1 - 10
of 327
pro vyhledávání: '"Mary Judge"'
Publikováno v:
BMJ Case Rep
A neonate was born with generalised, erythrodermic, thick, fissured skin, severe ectropion, hypoplastic auricles and limb abnormalities. A clinical diagnosis of harlequin ichthyosis was made, allowing supportive therapies to be commenced promptly. Or
Autor:
Jill Fenwick, Mark P Saunders, Abigail Garbutt, Michael Braun, Mary Judge, Theodora Germetaki, Nina Paton, Janette Beech, Joanne Collins
Publikováno v:
Future Oncology. 14:2531-2541
Cutaneous toxicities associated with EGFR inhibitors (EGFRIs) have a significant impact on patient treatment continuation, quality of life and healthcare resource utilization. This paper reviews the current prophylaxis and management of EGFRI-induced
Publikováno v:
International Journal of Paediatric Dentistry. 22:390-396
Background This paper aims to review the case of a girl who presented with a number of dental anomalies, in addition to unusual skin, nail and hair conditions. Tragically an undiagnosed cardiomyopathy caused unexpected sudden death. The case is discu
Autor:
Mary Judge, Robert Wynn, Anna Kelsey, Deepa R. J. Arachchillage, Bronwyn Kerr, Trevor F. Carr, Kay C. Hawkins
Publikováno v:
Journal of Pediatric Hematology/Oncology. 32:152-155
Juvenile xanthogranuloma (JXG) is rarely associated with either hemophagocytic lymphohistiocytosis (HLH) or juvenile myelomonocytic leukemia (JMML) and when in association with the latter there is usually neurofibromatosis type 1. We report a child w
Publikováno v:
International journal of paediatric dentistry. 22(5)
This paper aims to review the case of a girl who presented with a number of dental anomalies, in addition to unusual skin, nail and hair conditions. Tragically an undiagnosed cardiomyopathy caused unexpected sudden death. The case is discussed with r
Autor:
Fink, Lauren1,2,3 (AUTHOR) finkl1@mcmaster.ca, Fiehn, Hannah1,4 (AUTHOR), Wald-Fuhrmann, Melanie1,2 (AUTHOR)
Publikováno v:
Scientific Reports. 9/9/2024, Vol. 14 Issue 1, p1-9. 9p.
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 15(2)
Degos disease, or malignant atrophic papulosis, is a rare vasculopathy of uncertain aetiology manifesting as a primary dermatological disorder in most cases, but with widespread systemic involvement developing in an undefined proportion of patients.
Autor:
Kirsty J. Rutter, Mary Judge
Publikováno v:
Pediatric dermatology. 26(1)
Milia are keratin containing dermal cysts and are seen very frequently in neonates. They generally resolve spontaneously within the first few months of life. However, the presence of congenital milia may also be associated with a number of inherited
Autor:
Mary Judge
Publikováno v:
Clinical medicine (London, England). 5(6)