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

Year Number of Results
1957 1
1964 1
1966 2
1968 1
1969 1
1970 3
1971 1
1972 2
1973 4
1974 2
1975 2
1976 6
1977 4
1978 3
1979 5
1980 5
1981 7
1982 10
1983 8
1984 15
1985 9
1986 13
1987 12
1988 5
1989 18
1990 15
1991 10
1992 19
1993 9
1994 22
1995 19
1996 26
1997 28
1998 22
1999 22
2000 34
2001 30
2002 26
2003 35
2004 38
2005 32
2006 36
2007 48
2008 42
2009 43
2010 55
2011 51
2012 63
2013 62
2014 63
2015 55
2016 59
2017 58
2018 62
2019 53
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2022 59
2023 51
2024 10

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1,359 results

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Quoted phrase not found in phrase index: "Cafe-au-lait macules with pulmonary stenosis"
Page 1
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. ...
Pulmonary hypertension associated with neurofibromatosis type 1.
Jutant EM, Girerd B, Jaïs X, Savale L, O'Connell C, Perros F, Sitbon O, Humbert M, Montani D. Jutant EM, et al. Eur Respir Rev. 2018 Aug 29;27(149):180053. doi: 10.1183/16000617.0053-2018. Print 2018 Sep 30. Eur Respir Rev. 2018. PMID: 30158278 Free PMC article. Review.
PH-NF1 was characterised by a female predominance, an advanced age at diagnosis, an association with parenchymal lung disease in two out of three cases and poor long-term prognosis. NF1 is generally associated with interstitial lung disease but some cases of severe PH with …
PH-NF1 was characterised by a female predominance, an advanced age at diagnosis, an association with parenchymal lung disease in two out of …
Neurofibromatosis.
Frank-Stromborg M. Frank-Stromborg M. Semin Oncol Nurs. 1992 Nov;8(4):265-71. doi: 10.1016/0749-2081(92)90039-6. Semin Oncol Nurs. 1992. PMID: 1480857 Review.
Monogenic diseases in India.
Venugopal A, Chandran M, Eruppakotte N, Kizhakkillach S, Breezevilla SC, Vellingiri B. Venugopal A, et al. Mutat Res Rev Mutat Res. 2018 Apr-Jun;776:23-31. doi: 10.1016/j.mrrev.2018.03.003. Epub 2018 Mar 17. Mutat Res Rev Mutat Res. 2018. PMID: 29807575 Review.
Segmental neurofibromatosis and malignancy.
Dang JD, Cohen PR. Dang JD, et al. Skinmed. 2010 May-Jun;8(3):156-9. Skinmed. 2010. PMID: 21137621 Review.
Segmental neurofibromatosis is an uncommon variant of neurofibromatosis type I characterized by neurofibromas and/or cafe-au-lait macules localized to one sector of the body. Although patients with neurofibromatosis type I have an associated increased …
Segmental neurofibromatosis is an uncommon variant of neurofibromatosis type I characterized by neurofibromas and/or cafe-au- …
The pathoetiology of neurofibromatosis 1.
Jouhilahti EM, Peltonen S, Heape AM, Peltonen J. Jouhilahti EM, et al. Am J Pathol. 2011 May;178(5):1932-9. doi: 10.1016/j.ajpath.2010.12.056. Epub 2011 Mar 31. Am J Pathol. 2011. PMID: 21457932 Free PMC article. Review.
Although a mutation in the NF1 gene is the only factor required to initiate the neurocutaneous-skeletal neurofibromatosis 1 (NF1) syndrome, the pathoetiology of the multiple manifestations of this disease in different organ systems seems increasingly complex. ...The …
Although a mutation in the NF1 gene is the only factor required to initiate the neurocutaneous-skeletal neurofibromatosis 1 (N …
Diagnostic and follow-up protocol for adult patients with neurofibromatosis type 1 in a Spanish reference unit.
Solares I, Vinal D, Morales-Conejo M. Solares I, et al. Rev Clin Esp (Barc). 2022 Oct;222(8):486-495. doi: 10.1016/j.rceng.2022.02.007. Epub 2022 Jun 7. Rev Clin Esp (Barc). 2022. PMID: 35688675 Review.
Neurofibromatosis type 1 (NF1) is one of the most common genetic neurocutaneous disorders. The hallmark of this disease is skin lesions in the form of cafe-au-lait spots, ephelides, and the characteristic cutaneous neurofibromas. ...
Neurofibromatosis type 1 (NF1) is one of the most common genetic neurocutaneous disorders. The hallmark of this disease is skin lesions in t …
1,359 results