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 NCBI Filters

Results by year

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

Year Number of Results
1925 1
1934 3
1935 1
1937 1
1938 1
1942 1
1945 3
1946 6
1947 10
1948 6
1949 3
1950 16
1951 10
1952 15
1953 11
1954 17
1955 15
1956 14
1957 17
1958 14
1959 15
1960 16
1961 20
1962 17
1963 24
1964 30
1965 34
1966 34
1967 26
1968 27
1969 36
1970 37
1971 32
1972 33
1973 31
1974 45
1975 35
1976 41
1977 43
1978 43
1979 46
1980 46
1981 40
1982 43
1983 44
1984 34
1985 38
1986 36
1987 49
1988 45
1989 49
1990 47
1991 49
1992 47
1993 56
1994 44
1995 69
1996 54
1997 55
1998 50
1999 43
2000 60
2001 52
2002 53
2003 56
2004 56
2005 58
2006 76
2007 90
2008 76
2009 88
2010 101
2011 103
2012 81
2013 116
2014 100
2015 94
2016 83
2017 82
2018 97
2019 112
2020 116
2021 118
2022 99
2023 95
2024 53

Text availability

Article attribute

Article type

Publication date

Search Results

3,682 results

Results by year

Filters applied: . Clear all
Page 1
Klippel-Feil syndrome: a review of the literature.
Frikha R. Frikha R. Clin Dysmorphol. 2020 Jan;29(1):35-37. doi: 10.1097/MCD.0000000000000301. Clin Dysmorphol. 2020. PMID: 31577545 Review.
Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical spine. ...In this review, we focussed on clinical heterogeneity; radiographic abnormalities and genetic etiology in Klippel-Feil syndrome. We insist on comprehensive evalua …
Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical spine. ...In this review, we focussed o …
Klippel-Trenaunay Syndrome.
Suda T, Katagiri A, Fujii H. Suda T, et al. Intern Med. 2023 May 1;62(9):1377-1378. doi: 10.2169/internalmedicine.0251-22. Epub 2022 Sep 28. Intern Med. 2023. PMID: 36171122 Free PMC article. No abstract available.
Klippel-Feil syndrome.
McBride WZ. McBride WZ. Am Fam Physician. 1992 Feb;45(2):633-5. Am Fam Physician. 1992. PMID: 1739048 Review.
The triad of short neck, low posterior hairline and severe restriction of cervical motion is a classic definition of Klippel-Feil syndrome. The anatomic and clinical expressions of this syndrome vary widely, ranging from mild cosmetic deformity to severe disability. ...
The triad of short neck, low posterior hairline and severe restriction of cervical motion is a classic definition of Klippel-Feil syn …
The Klippel-Trenaunay Syndrome in 2022: Unravelling Its Genetic and Molecular Profile and Its Link to the Limb Overgrowth Syndromes.
Harnarayan P, Harnanan D. Harnarayan P, et al. Vasc Health Risk Manag. 2022 Apr 2;18:201-209. doi: 10.2147/VHRM.S358849. eCollection 2022. Vasc Health Risk Manag. 2022. PMID: 35401004 Free PMC article. Review.
The Klippel-Trenaunay syndrome is an unusual syndrome of vascular and dermatologic manifestation in which patients demonstrate hemihypertrophy of the soft tissue and bones of one limb, cutaneous haemangiomas and varicosities in anatomically abnormal positions. ...Several a …
The Klippel-Trenaunay syndrome is an unusual syndrome of vascular and dermatologic manifestation in which patients demonstrate hemihy …
Gastrointestinal involvement in Klippel-Trenaunay syndrome: pathophysiology, evaluation, and management.
Wang H, Lin W, Xie C, Yang W, Zhou J, Guo Z. Wang H, et al. Orphanet J Rare Dis. 2023 Sep 12;18(1):288. doi: 10.1186/s13023-023-02857-5. Orphanet J Rare Dis. 2023. PMID: 37700367 Free PMC article. Review.
Klippel-Trenaunay syndrome is typically a complex combined capillary-lymphatic-venous malformation in lower limb. Gastrointestinal involvement is not infrequent in Klippel-Trenaunay syndrome. Rectal bleeding is the most common complication. ...
Klippel-Trenaunay syndrome is typically a complex combined capillary-lymphatic-venous malformation in lower limb. Gastrointestinal in …
Klippel-Trenaunay syndrome.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet. 2000 Jul 31;93(3):171-5. doi: 10.1002/1096-8628(20000731)93:3<171::aid-ajmg1>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10925375 No abstract available.
Klippel-Feil Syndrome: Clinical Presentation and Management.
Jae-Min Park A, Nelson SE, Mesfin A. Jae-Min Park A, et al. JBJS Rev. 2022 Feb 15;10(2). doi: 10.2106/JBJS.RVW.21.00166. JBJS Rev. 2022. PMID: 35171878
": Klippel-Feil syndrome (KFS) is a rare multisystem constellation of findings with congenital cervical fusion as the hallmark. ...
": Klippel-Feil syndrome (KFS) is a rare multisystem constellation of findings with congenital cervical fusion as the hallmark. ...
Klippel-Trenaunay-Servelle syndrome in pediatrics.
Papendieck CM, Barbosa ML, Pozo P, Braun D, Vannelli C. Papendieck CM, et al. Lymphat Res Biol. 2003;1(1):81-4; discussion 85. doi: 10.1089/15396850360495745. Lymphat Res Biol. 2003. PMID: 15624326 Review.
The aim of this report is to explain the historical differences between Klippel-Trenaunay (KT), Klippel-Trenaunay-Weber (KTW), and Klippel-Trenaunay-Servelle (KTS) syndromes. ...
The aim of this report is to explain the historical differences between Klippel-Trenaunay (KT), Klippel-Trenaunay-Weber (KTW), …
Klippel-Trenaunay-Weber syndrome.
Meine JG, Schwartz RA, Janniger CK. Meine JG, et al. Cutis. 1997 Sep;60(3):127-32. Cutis. 1997. PMID: 9314616 Review.
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue hypertrophy of an extremity. ...We will review the clinical features, etiology, assessment, and treatment of patients with Klippel-Trena …
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue hyp …
Klippel-Trenaunay syndrome: current management.
Gloviczki P, Driscoll DJ. Gloviczki P, et al. Phlebology. 2007;22(6):291-8. doi: 10.1177/026835550702200611. Phlebology. 2007. PMID: 18274338 Review.
Klippel-Trenaunay syndrome (KTS) is a rare, sporadic, complex malformation characterized by the clinical triad of (1) capillary malformations (port wine stain); (2) soft tissue and bone hypertrophy or, occasionally, hypotrophy of usually one lower limb; and (3) atypical, m …
Klippel-Trenaunay syndrome (KTS) is a rare, sporadic, complex malformation characterized by the clinical triad of (1) capillary malfo …
3,682 results