Phenotype and Course of Hutchinson-Gilford Progeria Syndrome
- Author
- MERIDETH, Melissa A1 2 ; GORDON, Leslie B3 ; BROOKS, Brian P9 ; GERBER, Lynn H10 ; TURNER, Maria L11 ; DOMINGO, Demetrio L12 ; HART, Thomas C12 ; GRAF, Jennifer13 ; REYNOLDS, James C14 ; GROPMAN, Andrea1 4 ; YANOVSKI, Jack A15 ; GERHARD-HERMAN, Marie16 ; CLAUSS, Sarah4 ; COLLINS, Francis S1 ; NABEL, Elizabeth G5 ; CANNON, Richard O5 ; GAHL, William A1 ; INTRONE, Wendyj1 ; SACHDEV, Vandana5 ; SMITH, Ann C. M6 ; PERRY, Monique B7 ; BREWER, Carmen C8 ; ZALEWSKI, Christopher8 ; KIM, H. Jeffrey8 ; SOLOMON, Beth7
[1] National Human Genome Research Institute, United States
[2] Intramural Office of Rare Disease, Office of the Director, National Institutes of Health, United States
[3] Brown University, Providence, RI, United States
[4] Children's National Medical Center, United States
[5] National Heart, Lung, and Blood Institute, United States
[6] Georgetown University Medical Center, Washington, DC, United States
[7] Department of Rehabilitation Medicine, Warren Alpert Medical School, Bethesda, MD, United States
[8] Department of Clinical Center, National Institutes of Health; National Institute on Deafness and Other Communication Disorders, Warren Alpert Medical School, Bethesda, MD, United States
[9] Department of National Eye Institute, Warren Alpert Medical School, Bethesda, MD, United States
[10] Center for Chronic Illness and Disability, George Mason University, Fairfax, VA, United States
[11] Department of National Cancer Institute, Warren Alpert Medical School, Bethesda, MD, United States
[12] Department of National Institute of Dental and Craniofacial Research, Warren Alpert Medical School, Bethesda, MD, United States
[13] Department of Nutrition, Warren Alpert Medical School, Bethesda, MD, United States
[14] Department of Nuclear Medicine, Warren Alpert Medical School, Bethesda, MD, United States
[15] Department of National Institute of Child Health and Human Development, Warren Alpert Medical School, Bethesda, MD, United States
[16] Brigham and Women's Hospital, Boston, United States - Source
The New England journal of medicine. 2008, Vol 358, Num 6, pp 592-604, 13 p ; ref : 42 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Boston, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Médecine Phénotype Progéria Syndrome Nanisme Pathologie de la peau
- Keyword (en)
- Medicine Phenotype Progeria Syndrome Dwarfism Skin disease
- Keyword (es)
- Medicina Fenotipo Progería Síndrome Enanismo Piel patología
- Classification
- Discipline
- Generalities in medical sciences
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20057788
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1056/NEJMoa0706898 
https://dx.doi.org/10.1056/NEJMoa0706898
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