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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 1
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1953 1
1954 1
1955 1
1962 1
1963 1
1964 4
1966 5
1967 9
1968 12
1969 7
1970 17
1971 13
1972 13
1973 12
1974 8
1975 17
1976 22
1977 14
1978 19
1979 19
1980 16
1981 33
1982 24
1983 25
1984 40
1985 34
1986 32
1987 52
1988 56
1989 81
1990 46
1991 40
1992 48
1993 39
1994 42
1995 43
1996 45
1997 56
1998 49
1999 55
2000 73
2001 64
2002 75
2003 78
2004 81
2005 79
2006 99
2007 113
2008 96
2009 106
2010 135
2011 114
2012 150
2013 166
2014 141
2015 139
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2017 125
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2023 145
2024 41

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3,577 results

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Quoted phrase not found in phrase index: "Cafe-au-lait macules with pulmonary stenosis"
Page 1
Neurofibromatosis type 1.
Cimino PJ, Gutmann DH. Cimino PJ, et al. Handb Clin Neurol. 2018;148:799-811. doi: 10.1016/B978-0-444-64076-5.00051-X. Handb Clin Neurol. 2018. PMID: 29478615 Review.
Health Supervision for Children With Neurofibromatosis Type 1.
Miller DT, Freedenberg D, Schorry E, Ullrich NJ, Viskochil D, Korf BR; COUNCIL ON GENETICS; AMERICAN COLLEGE OF MEDICAL GENETICS AND GENOMICS. Miller DT, et al. Pediatrics. 2019 May;143(5):e20190660. doi: 10.1542/peds.2019-0660. Pediatrics. 2019. PMID: 31010905 Review.
Neurofibromatosis type 1 (NF1): diagnosis and management.
Ferner RE, Gutmann DH. Ferner RE, et al. Handb Clin Neurol. 2013;115:939-55. doi: 10.1016/B978-0-444-52902-2.00053-9. Handb Clin Neurol. 2013. PMID: 23931823 Review.
Neurofibromatosis 1 (NF1) is an inherited neurocutaneous disease that has a major impact on the nervous system, eye, skin, and bone. ...
Neurofibromatosis 1 (NF1) is an inherited neurocutaneous disease that has a major impact on the nervous system, eye, skin, and
Guidelines for the diagnosis and management of individuals with neurofibromatosis 1.
Ferner RE, Huson SM, Thomas N, Moss C, Willshaw H, Evans DG, Upadhyaya M, Towers R, Gleeson M, Steiger C, Kirby A. Ferner RE, et al. J Med Genet. 2007 Feb;44(2):81-8. doi: 10.1136/jmg.2006.045906. Epub 2006 Nov 14. J Med Genet. 2007. PMID: 17105749 Free PMC article. Review.
Neurofibromatosis 1 (NF1) is a common neurocutaneous condition with an autosomal dominant pattern of inheritance. ...
Neurofibromatosis 1 (NF1) is a common neurocutaneous condition with an autosomal dominant pattern of inheritance. ...
An update on the central nervous system manifestations of neurofibromatosis type 1.
Nix JS, Blakeley J, Rodriguez FJ. Nix JS, et al. Acta Neuropathol. 2020 Apr;139(4):625-641. doi: 10.1007/s00401-019-02002-2. Epub 2019 Apr 8. Acta Neuropathol. 2020. PMID: 30963251 Free PMC article. Review.
Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder that presents with variable phenotypes as a result of mutations in the neurofibromatosis type 1 (NF1) gene and subsequently, abnormal function of the protein product, neurofibromin. ...A variety of
Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder that presents with variable phenotypes as a result of muta
The NF1 somatic mutational landscape in sporadic human cancers.
Philpott C, Tovell H, Frayling IM, Cooper DN, Upadhyaya M. Philpott C, et al. Hum Genomics. 2017 Jun 21;11(1):13. doi: 10.1186/s40246-017-0109-3. Hum Genomics. 2017. PMID: 28637487 Free PMC article. Review.
NF1 exhibits variable clinical expression and is characterized by benign cutaneous lesions including neurofibromas and cafe-au-lait macules, as well as a predisposition to various types of malignancy, such as breast cancer and leukaemia. ...
NF1 exhibits variable clinical expression and is characterized by benign cutaneous lesions including neurofibromas and cafe-au
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants.
Kehrer-Sawatzki H, Cooper DN. Kehrer-Sawatzki H, et al. Hum Genet. 2022 Feb;141(2):177-191. doi: 10.1007/s00439-021-02410-z. Epub 2021 Dec 20. Hum Genet. 2022. PMID: 34928431 Free PMC article. Review.
Neurofibromatosis type 1 (NF1) is the most frequent disorder associated with multiple cafe-au-lait macules (CALM) which may either be present at birth or appear during the first year of life. ...
Neurofibromatosis type 1 (NF1) is the most frequent disorder associated with multiple cafe-au-lait macules (CALM …
3,577 results