نتایج جستجو برای: phakomatosis pigmentovascularis
تعداد نتایج: 132 فیلتر نتایج به سال:
Cutis. 2007;80:284-8. 13. Cheadle JP, Reeve MP, Sampson JR, Kwiatkowski DJ. Molecular genetic advances in tuberous sclerosis. Hum Genet. 2000;107:97-114. 14. Darling TN, Skarulis MC, Steinberg SM, Marx SJ, Spiegel AM, Turner M. Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1. Arch Dermatol. 1997;133:853-7. 15. Phillips CM, Rye B. Neurofibromat...
Vol. 27, No. 3, 2015 353 Received April 23, 2014, Revised July 22, 2014, Accepted for publication August 11, 2014 Corresponding author: Hei Sung Kim, Department of Dermatology, The Catholic University of Korea, Incheon St. Mary’s Hospital, 56 Dongsuro, Bupyoung-gu, Incheon 403-720, Korea. Tel: 82-32-2805102, Fax: 82-32-506-9514, E-mail: [email protected] This is an Open Access article dist...
DEAR EDITOR, Infantile haemangioma (IH) is a very common benign vascular tumour with a reported incidence of 4–10% in infants, and no clear genetic basis described as yet. Congenital melanocytic naevi (CMN) are benign melanocytic tumours present in 1% of newborns, which when multiple are caused by post-zygotic mutations in the gene NRAS in the majority of cases, and when single, carry various s...
We read with interest the report by Moxey-Mims et aI., "Increased Incidence of Insulin-Dependent Diabetes Mellitus in Pediatric Renal Transplant Patients Receiving Tacrolimus (FK506)," reporting a 100% incidence of posttransplant diabetes mellitus in five pediatric patients receiving tacrolimusbased immunosuppression after renal transplantation (1). Although posttransplant diabetes mellitus (PT...
9.6 mg/dL, serum phosphate: 1.8mg/dL; alkaline phosphatase: 982 U/L. Acid load test was negative. TMP/GFR: 0.5, Magnetic resonance imaging of the brain showed interdigitation of gyri in the right frontal lobe. X-ray showed changes of rickets. Biopsy of the skin lesion was suggestive of epidermal nevus. He was started on phosphate mixture Sanklecha M, Singhal S, et al. Hereditory spherocytosis: ...
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