Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1964 2
1965 1
1967 2
1970 4
1977 1
1984 3
1986 2
1987 5
1988 4
1989 6
1990 5
1991 5
1992 6
1993 5
1994 2
1995 6
1996 4
1997 4
1998 3
1999 6
2000 5
2001 2
2002 1
2003 1
2004 3
2005 2
2006 2
2007 4
2008 8
2009 3
2010 11
2011 8
2012 7
2013 12
2014 17
2015 16
2016 15
2017 15
2018 18
2019 23
2020 19
2021 14
2022 9
2023 5
2024 11

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

279 results

Results by year

Filters applied: . Clear all
Page 1
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.
Health Supervision for People With Achondroplasia.
Hoover-Fong J, Scott CI, Jones MC; COMMITTEE ON GENETICS. Hoover-Fong J, et al. Pediatrics. 2020 Jun;145(6):e20201010. doi: 10.1542/peds.2020-1010. Pediatrics. 2020. PMID: 32457214 Review.
Health Supervision for Children and Adolescents With Down Syndrome.
Bull MJ, Trotter T, Santoro SL, Christensen C, Grout RW; COUNCIL ON GENETICS; Burke LW, Berry SA, Geleske TA, Holm I, Hopkin RJ, Introne WJ, Lyons MJ, Monteil DC, Scheuerle A, Stoler JM, Vergano SA, Chen E, Hamid R, Downs SM, Grout RW, Cunniff C, Parisi MA, Ralston SJ, Scott JA, Shapira SK, Spire P. Bull MJ, et al. Among authors: berry sa. Pediatrics. 2022 May 1;149(5):e2022057010. doi: 10.1542/peds.2022-057010. Pediatrics. 2022. PMID: 35490285 No abstract available.
Phenylalanine hydroxylase deficiency: diagnosis and management guideline.
Vockley J, Andersson HC, Antshel KM, Braverman NE, Burton BK, Frazier DM, Mitchell J, Smith WE, Thompson BH, Berry SA; American College of Medical Genetics and Genomics Therapeutics Committee. Vockley J, et al. Among authors: berry sa. Genet Med. 2014 Feb;16(2):188-200. doi: 10.1038/gim.2013.157. Epub 2013 Oct 10. Genet Med. 2014. PMID: 24385074 Free article.
Early prediction of phenotypic severity in Citrullinemia Type 1.
Zielonka M, Kölker S, Gleich F, Stützenberger N, Nagamani SCS, Gropman AL, Hoffmann GF, Garbade SF, Posset R; Urea Cycle Disorders Consortium (UCDC) and the European Registry and Network for Intoxication type Metabolic Diseases (E-IMD) Consortia Study Group. Zielonka M, et al. Ann Clin Transl Neurol. 2019 Sep;6(9):1858-1871. doi: 10.1002/acn3.50886. Epub 2019 Aug 30. Ann Clin Transl Neurol. 2019. PMID: 31469252 Free PMC article.
Newborn screening.
Berry SA. Berry SA. Clin Perinatol. 2015 Jun;42(2):441-53, x. doi: 10.1016/j.clp.2015.03.002. Epub 2015 Apr 4. Clin Perinatol. 2015. PMID: 26042913 Review.
Professional Relations.
Turner JW, Barata I, Berry SA, Bruce DA, Crandall LG, Gunther WM, Kay AJ, Landi K. Turner JW, et al. Among authors: berry sa. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 13. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 13. PMID: 35107916 Free Books & Documents. Review. No abstract available.
Klippel-Trenaunay syndrome.
Berry SA, Peterson C, Mize W, Bloom K, Zachary C, Blasco P, Hunter D. Berry SA, et al. Am J Med Genet. 1998 Oct 2;79(4):319-26. Am J Med Genet. 1998. PMID: 9781914 Review.
Evaluation for Genetic and Metabolic Disorders.
Bundock EA, Ackerman MJ, Berry SA, Landi K, Matshes EW, Williams N. Bundock EA, et al. Among authors: berry sa. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 9. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 9. PMID: 35107917 Free Books & Documents. Review. No abstract available.
279 results