Error in a Study of the Clinical and Mutational Spectrum of Neurofibromatosis Type 1-like Syndrome

被引:1
|
作者
Messiaen, Ludwine [1 ]
Legius, Eric [2 ]
机构
[1] Univ Alabama Birmingham, Dept Genet, Birmingham, AL 35294 USA
[2] Catholic Univ Louvain, Dept Human Genet, B-3000 Louvain, Belgium
来源
关键词
D O I
10.1001/jama.2010.827
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:2476 / 2477
页数:2
相关论文
共 50 条
  • [41] Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene
    Upadhyaya, M
    Osborn, MJ
    Maynard, J
    Kim, MR
    Tamanoi, F
    Cooper, DN
    HUMAN GENETICS, 1997, 99 (01) : 88 - 92
  • [42] Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients
    Lazaro, C
    Gaona, A
    Ainsworth, P
    Tenconi, R
    Vidaud, D
    Kruyer, H
    Ars, E
    Volpini, V
    Estivill, X
    HUMAN GENETICS, 1996, 98 (06) : 696 - 699
  • [43] Delineating Visual Habituation Profiles in Preschoolers with Neurofibromatosis Type 1 and Autism Spectrum Disorder: A Cross-Syndrome Study
    Hocking, Darren R.
    Sun, Xiaoyun
    Haebich, Kristina
    Darke, Hayley
    North, Kathryn N.
    Vivanti, Giacomo
    Payne, Jonathan M.
    JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2024, 54 (05) : 1998 - 2011
  • [44] Erythropoietin ameliorates hyperglycemia in type 1-like diabetic rats
    Niu, Ho-Shan
    Chang, Chin-Hong
    Niu, Chiang-Shan
    Cheng, Juei-Tang
    Lee, Kung-Shing
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2016, 10 : 1877 - 1884
  • [45] Regarding "Vascular abnormalities in patients with neurofibromatosis syndrome type I: Clinical spectrum, management, and results" - Reply
    Oderich, Gustavo S.
    JOURNAL OF VASCULAR SURGERY, 2008, 47 (06) : 1379 - 1379
  • [46] Frey syndrome in a child with neurofibromatosis type 1
    Aragones Red, Maria
    Martinez Beneyto, Paz
    Marco, Jaime
    ACTA OTORRINOLARINGOLOGICA ESPANOLA, 2020, 71 (01): : 56 - 58
  • [47] Joubert Syndrome with Nephronophthisis in Neurofibromatosis Type 1
    Ahmed, Javed
    Ali, Uma S.
    SAUDI JOURNAL OF KIDNEY DISEASES AND TRANSPLANTATION, 2011, 22 (04) : 788 - 791
  • [48] Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome
    Belge, Hendrica
    Dahan, Karin
    Cambier, Jean-Francois
    Benoit, Valerie
    Morelle, Johann
    Bloch, Julie
    Vanhille, Philippe
    Pirson, Yves
    Demoulin, Nathalie
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32 (05) : 830 - 837
  • [49] Tourette's syndrome and neurofibromatosis type 1
    Cosentino, C
    Torres, L
    PEDIATRIC NEUROLOGY, 2000, 22 (05) : 420 - 421
  • [50] Joubert's Syndrome and neurofibromatosis type 1
    Esther Vazquez-Lopez, M.
    Silveira-Cancela, Manuel
    Loidi-Fernandez, Lourdes
    Perez-Gay, Laura
    Pena-Gil, Patricia
    Juberias-Alzueta, Cristina
    Perez Pacin, Roberto
    REVISTA DE NEUROLOGIA, 2022, 74 (09) : 312 - 313