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

Year Number of Results
1831 1
1952 2
1953 2
1954 1
1955 4
1956 1
1957 4
1958 8
1959 19
1960 15
1961 16
1962 14
1963 36
1964 31
1965 29
1966 35
1967 34
1968 28
1969 27
1970 32
1971 37
1972 36
1973 24
1974 45
1975 47
1976 24
1977 28
1978 21
1979 23
1980 30
1981 19
1982 24
1983 22
1984 23
1985 29
1986 32
1987 32
1988 33
1989 43
1990 43
1991 42
1992 42
1993 46
1994 39
1995 50
1996 50
1997 43
1998 43
1999 40
2000 43
2001 49
2002 48
2003 36
2004 45
2005 51
2006 57
2007 59
2008 59
2009 60
2010 53
2011 55
2012 74
2013 83
2014 86
2015 90
2016 59
2017 76
2018 74
2019 74
2020 78
2021 106
2022 62
2023 71
2024 78
2025 58

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2,824 results

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Page 1
The consequences of hypoglycaemia.
Amiel SA. Amiel SA. Diabetologia. 2021 May;64(5):963-970. doi: 10.1007/s00125-020-05366-3. Epub 2021 Feb 7. Diabetologia. 2021. PMID: 33550443 Free PMC article. Review.
The Amiel-Tison Neurological Assessment at Term: conceptual and methodological continuity in the course of follow-up.
Gosselin J, Gahagan S, Amiel-Tison C. Gosselin J, et al. Ment Retard Dev Disabil Res Rev. 2005;11(1):34-51. doi: 10.1002/mrdd.20049. Ment Retard Dev Disabil Res Rev. 2005. PMID: 15856442 Review.
The Amiel-Tison Neurological Assessment at Term (ATNAT) is part of a set of three different instruments based on a neuro-maturative framework. ...
The Amiel-Tison Neurological Assessment at Term (ATNAT) is part of a set of three different instruments based on a neuro-maturative f …
A case of Chopra-Amiel-Gordon syndrome with a novel heterozygous variant in the ANKRD17 gene: A case report.
Tinatin T, Kakha B, Mikheil G, Tamari SD, Elene A. Tinatin T, et al. SAGE Open Med Case Rep. 2023 Jul 10;11:2050313X231186496. doi: 10.1177/2050313X231186496. eCollection 2023. SAGE Open Med Case Rep. 2023. PMID: 37456926 Free PMC article.
Chopra-Amiel-Gordon syndrome (OMIM: 619504) is an autosomal dominant neurodevelopmental disorder characterized by developmental delay, intellectual disability, speech delay, epilepsy, dysmorphic craniofacial features, ophthalmological abnormalities, and recurrent infection …
Chopra-Amiel-Gordon syndrome (OMIM: 619504) is an autosomal dominant neurodevelopmental disorder characterized by developmental delay …
[Immunosuppression].
Amiel JL. Amiel JL. Minerva Med. 1970 Jul 11;61(55):3022-7. Minerva Med. 1970. PMID: 5427676 Italian. No abstract available.
"Brittle" diabetes.
Amiel SA. Amiel SA. BMJ. 1991 Aug 3;303(6797):260-1. doi: 10.1136/bmj.303.6797.260. BMJ. 1991. PMID: 1888921 Free PMC article. No abstract available.
ANKRD17-Related Neurodevelopmental Syndrome.
Sveden A, Gordon CT, Amiel J, Chopra M. Sveden A, et al. 2022 Dec 22. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2022 Dec 22. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 36548456 Free Books & Documents. Review.
A review of the Amiel-Tison neurologic evaluation of the newborn and infant.
McCarraher-Wetzel AP, Wetzel RC. McCarraher-Wetzel AP, et al. Am J Occup Ther. 1984 Sep;38(9):585-93. doi: 10.5014/ajot.38.9.585. Am J Occup Ther. 1984. PMID: 6486239
Because occupational therapists are becoming more involved in infant assessment and intervention, there is a need for objective, prospective, and serially applicable evaluation tools. Amiel-Tison's Neurologic Evaluation of the Newborn and the Infant provides such a tool fo …
Because occupational therapists are becoming more involved in infant assessment and intervention, there is a need for objective, prospective …
[In memoriam. Claudine Amiel-Tison].
Garcia-Alix A, Demestre X. Garcia-Alix A, et al. An Pediatr (Barc). 2014 Dec;81(6):e74-5. doi: 10.1016/j.anpedi.2014.05.021. An Pediatr (Barc). 2014. PMID: 25625148 Spanish. No abstract available.
[Immunodepression].
Amiel JL. Amiel JL. Cah Med. 1970 May 15;11(5):383-8. Cah Med. 1970. PMID: 4912852 French. No abstract available.
2,824 results