Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1.
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Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1. / Lammert, M; Friedman, J M; Roth, H J; Friedrich, Reinhard; Kluwe, Lan; Atkins, D; Schooler, T; Mautner, Viktor Felix.
In: J MED GENET, Vol. 43, No. 10, 10, 2006, p. 810-813.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1.
AU - Lammert, M
AU - Friedman, J M
AU - Roth, H J
AU - Friedrich, Reinhard
AU - Kluwe, Lan
AU - Atkins, D
AU - Schooler, T
AU - Mautner, Viktor Felix
PY - 2006
Y1 - 2006
N2 - Neurofibromatosis 1 (NF1) is a tumour suppressor gene syndrome characterized by multiple cutaneous and plexiform neurofibromas. Focal osseous abnormalities, short stature, and decreased bone mineral density are also frequent in people with NF1. We measured serum 25-hydroxyvitamin D concentrations in 55 patients with NF1 and 58 healthy controls, and correlated the findings in the patients with NF1 with their estimated number of dermal neurofibromas. Geometric mean (SD) serum 25-hydroxyvitamin D concentration was 14.0 (1.6) ng/mL among the patients with NF1 compared with 31.4 (1.7) ng/mL among healthy controls (p
AB - Neurofibromatosis 1 (NF1) is a tumour suppressor gene syndrome characterized by multiple cutaneous and plexiform neurofibromas. Focal osseous abnormalities, short stature, and decreased bone mineral density are also frequent in people with NF1. We measured serum 25-hydroxyvitamin D concentrations in 55 patients with NF1 and 58 healthy controls, and correlated the findings in the patients with NF1 with their estimated number of dermal neurofibromas. Geometric mean (SD) serum 25-hydroxyvitamin D concentration was 14.0 (1.6) ng/mL among the patients with NF1 compared with 31.4 (1.7) ng/mL among healthy controls (p
M3 - SCORING: Zeitschriftenaufsatz
VL - 43
SP - 810
EP - 813
JO - J MED GENET
JF - J MED GENET
SN - 0022-2593
IS - 10
M1 - 10
ER -