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

Year Number of Results
1916 1
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1948 3
1949 3
1950 1
1951 1
1952 1
1954 2
1955 1
1956 1
1957 2
1958 4
1959 3
1960 6
1961 9
1962 1
1963 8
1964 7
1965 9
1966 2
1967 9
1968 12
1969 10
1970 12
1971 7
1972 14
1973 28
1974 32
1975 30
1976 30
1977 35
1978 39
1979 50
1980 45
1981 37
1982 44
1983 39
1984 29
1985 47
1986 53
1987 78
1988 44
1989 44
1990 48
1991 59
1992 66
1993 65
1994 50
1995 74
1996 91
1997 71
1998 79
1999 78
2000 81
2001 83
2002 98
2003 107
2004 99
2005 131
2006 140
2007 163
2008 150
2009 201
2010 215
2011 200
2012 251
2013 256
2014 262
2015 301
2016 298
2017 296
2018 317
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2020 369
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2023 366
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7,041 results

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Page 1
Noonan's syndrome.
[No authors listed] [No authors listed] Lancet. 1992 Jul 4;340(8810):22-3. Lancet. 1992. PMID: 1351605 No abstract available.
Noonan's syndrome.
Agarwal B, Guha D, Banerjee D. Agarwal B, et al. J Indian Med Assoc. 1999 Dec;97(12):524. J Indian Med Assoc. 1999. PMID: 10638133 No abstract available.
[Noonan's syndrome].
Guibaud P. Guibaud P. Pediatrie. 1969 Mar;24(2):221-4. Pediatrie. 1969. PMID: 4901597 Review. French. No abstract available.
The other side of Turner's: Noonan's syndrome.
Agarwal P, Philip R, Gutch M, Gupta KK. Agarwal P, et al. Indian J Endocrinol Metab. 2013 Sep;17(5):794-8. doi: 10.4103/2230-8210.117197. Indian J Endocrinol Metab. 2013. PMID: 24083159 Free PMC article. Review.
Noonan Syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical face dysmorphology, and congenital heart defects. ...
Noonan Syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical face dysmorphology, and congenital hea …
Clinical overview on RASopathies.
Zenker M. Zenker M. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):414-424. doi: 10.1002/ajmg.c.32015. Epub 2022 Nov 25. Am J Med Genet C Semin Med Genet. 2022. PMID: 36428239 Review.
RASopathies comprise a group of clinically overlapping developmental disorders caused by genetic variations affecting components or modulators of the RAS-MAPK signaling cascade, which lead to dysregulation of signal flow through this pathway. Noonan syndrome and the less f …
RASopathies comprise a group of clinically overlapping developmental disorders caused by genetic variations affecting components or modulato …
Juvenile myelomonocytic leukemia-A comprehensive review and recent advances in management.
Gupta AK, Meena JP, Chopra A, Tanwar P, Seth R. Gupta AK, et al. Am J Blood Res. 2021 Feb 15;11(1):1-21. eCollection 2021. Am J Blood Res. 2021. PMID: 33796386 Free PMC article. Review.
Karyotype abnormalities and additional epigenetic alterations can also be found in JMML. Neurofibromatosis and Noonan's syndrome have a predisposition for JMML. In a few patients, the RAS genes (NRAS, KRAS, and PTPN11) are mutated at the germline and this usually re …
Karyotype abnormalities and additional epigenetic alterations can also be found in JMML. Neurofibromatosis and Noonan's syndro …
Noonan's syndrome associated with polycistic renal disease.
Tejani A, Del Rosario C, Arulanantham K, Alpert LI. Tejani A, et al. J Urol. 1976 Feb;115(2):209-11. doi: 10.1016/s0022-5347(17)59134-x. J Urol. 1976. PMID: 765504 Review.
Noonan's syndrome is an eponymic designation that has been used during the last 8 years to describe a variable constellation of somatic and visceral congenital anomalies, which includes groups of patients previously referred to as male Turner's, female pseudo-Turner …
Noonan's syndrome is an eponymic designation that has been used during the last 8 years to describe a variable constellation o …
Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data.
Lamouroux A, Dauge C, Wells C, Mousty E, Pinson L, Cavé H, Capri Y, Faure JM, Grosjean F, Sauvestre F, Attié-Bitach T, Pelluard F, Geneviève D. Lamouroux A, et al. Prenat Diagn. 2022 May;42(5):574-582. doi: 10.1002/pd.6133. Epub 2022 Mar 22. Prenat Diagn. 2022. PMID: 35278234
OBJECTIVES: The antenatal phenotypic spectrum of Noonan Syndrome (NS) requires better characterization. METHODS: This multicenter retrospective observational included 16 fetuses with molecularly confirmed NS admitted for fetopathological examination between 2009 and 2016. …
OBJECTIVES: The antenatal phenotypic spectrum of Noonan Syndrome (NS) requires better characterization. METHODS: This multicenter ret …
7,041 results