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

Year Number of Results
1939 2
1942 1
1943 1
1944 2
1945 9
1946 15
1947 10
1948 21
1949 20
1950 12
1951 13
1952 14
1953 13
1954 11
1955 16
1956 11
1957 6
1958 10
1959 11
1960 10
1961 9
1962 14
1963 11
1964 18
1965 18
1966 17
1967 20
1968 26
1969 25
1970 24
1971 39
1972 28
1973 30
1974 23
1975 34
1976 27
1977 30
1978 26
1979 30
1980 29
1981 33
1982 35
1983 36
1984 58
1985 56
1986 51
1987 56
1988 61
1989 58
1990 55
1991 45
1992 52
1993 62
1994 52
1995 74
1996 54
1997 61
1998 78
1999 77
2000 80
2001 99
2002 74
2003 70
2004 102
2005 95
2006 93
2007 97
2008 86
2009 120
2010 118
2011 112
2012 146
2013 153
2014 161
2015 197
2016 212
2017 226
2018 243
2019 191
2020 261
2021 266
2022 230
2023 199
2024 85

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5,014 results

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The following term was not found in PubMed: Jacquelline
Page 1
Hands.
Perlman MH. Perlman MH. HCA Healthc J Med. 2021 Feb 26;2(1):71-72. doi: 10.36518/2689-0216.1212. eCollection 2021. HCA Healthc J Med. 2021. PMID: 37424891 Free PMC article.
[Perlman syndrome research progress].
Wang Z, Liu J, Yang Y. Wang Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Oct 10;38(10):1021-1024. doi: 10.3760/cma.j.cn511374-20200717-00525. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34625946 Chinese.
Perlman syndrome is a rare autosomal recessive congenital overgrowth syndrome caused by pathogenic variants of the DIS3L2 gene at 2q37 region. ...
Perlman syndrome is a rare autosomal recessive congenital overgrowth syndrome caused by pathogenic variants of the DIS3L2 gene at 2q3
Another Decade, Another Coronavirus.
Perlman S. Perlman S. N Engl J Med. 2020 Feb 20;382(8):760-762. doi: 10.1056/NEJMe2001126. Epub 2020 Jan 24. N Engl J Med. 2020. PMID: 31978944 Free PMC article. No abstract available.
Overgrowth Syndromes.
Edmondson AC, Kalish JM. Edmondson AC, et al. J Pediatr Genet. 2015 Sep;4(3):136-43. doi: 10.1055/s-0035-1564440. Epub 2015 Sep 25. J Pediatr Genet. 2015. PMID: 27617124 Free PMC article. Review.
We review syndromes such as Sotos, Malan, Marshall-Smith, Weaver, Simpson-Golabi-Behmel, Perlman, Bannayan-Riley-Ruvalcaba, PI3K-related, Proteus, Beckwith-Wiedemann, fibrous dysplasia, Klippel-Trenaunay-Weber, and Maffucci....
We review syndromes such as Sotos, Malan, Marshall-Smith, Weaver, Simpson-Golabi-Behmel, Perlman, Bannayan-Riley-Ruvalcaba, PI3K-rela …
Perlman syndrome: report, prenatal findings and review.
Alessandri JL, Cuillier F, Ramful D, Ernould S, Robin S, de Napoli-Cocci S, Rivière JP, Rossignol S. Alessandri JL, et al. Am J Med Genet A. 2008 Oct 1;146A(19):2532-7. doi: 10.1002/ajmg.a.32391. Am J Med Genet A. 2008. PMID: 18780370 Review.
We report on a newborn with prenatal sonographic signs of Perlman syndrome, large fetal ascites, nephromegaly and macrosomia. ...No mutation of the GPC3 gene was identified. We review the 28 patients who have been reported with Perlman syndrome. The prognosis of …
We report on a newborn with prenatal sonographic signs of Perlman syndrome, large fetal ascites, nephromegaly and macrosomia. ...No m …
SENSORINEURAL DEAFNESS.
PERLMAN HB. PERLMAN HB. Arch Otolaryngol. 1965 Sep;82:322-4. doi: 10.1001/archotol.1965.00760010324024. Arch Otolaryngol. 1965. PMID: 14327040 Review. No abstract available.
Cervical spondylolisthesis.
PERLMAN R, HAWES LE. PERLMAN R, et al. J Bone Joint Surg Am. 1951 Oct;33-A(4):1012-3. J Bone Joint Surg Am. 1951. PMID: 14880558 No abstract available.
Acoustic trauma.
PERLMAN HB. PERLMAN HB. Ann Surg. 1945;122:1086-91. Ann Surg. 1945. PMID: 21005207 No abstract available.
Actinomycin lactonase.
Perlman D. Perlman D. Methods Enzymol. 1975;43:763-7. doi: 10.1016/0076-6879(75)43144-5. Methods Enzymol. 1975. PMID: 49002 No abstract available.
5,014 results