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Year Number of Results
1946 3
1947 2
1948 3
1949 2
1950 5
1951 4
1952 3
1953 3
1954 2
1955 5
1956 10
1957 8
1958 7
1959 8
1960 6
1961 9
1962 17
1963 25
1964 30
1965 46
1966 65
1967 72
1968 89
1969 104
1970 138
1971 180
1972 181
1973 241
1974 318
1975 708
1976 736
1977 730
1978 776
1979 854
1980 876
1981 943
1982 1052
1983 1353
1984 1682
1985 2014
1986 2229
1987 2476
1988 2873
1989 3385
1990 3527
1991 3828
1992 3982
1993 4348
1994 4646
1995 4863
1996 5117
1997 5369
1998 5810
1999 5955
2000 6084
2001 6567
2002 7014
2003 7943
2004 8725
2005 10142
2006 10903
2007 11697
2008 12843
2009 13538
2010 14592
2011 15612
2012 16836
2013 18169
2014 18621
2015 18964
2016 19436
2017 19835
2018 20251
2019 20905
2020 26625
2021 29148
2022 26633
2023 22703
2024 7222

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407,800 results

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Quoted phrase not found in phrase index: "Epilepsy-telangiectasia syndrome"
Page 1
Understanding COPD-overlap syndromes.
Poh TY, Mac Aogáin M, Chan AK, Yii AC, Yong VF, Tiew PY, Koh MS, Chotirmall SH. Poh TY, et al. Expert Rev Respir Med. 2017 Apr;11(4):285-298. doi: 10.1080/17476348.2017.1305895. Epub 2017 Mar 24. Expert Rev Respir Med. 2017. PMID: 28282995 Review.
This is coined asthma-COPD overlap syndrome ('ACOS'). Other examples of such overlapping clinical states include bronchiectasis-COPD ('BCOS'), fibrosis-COPD ('FCOS') and OSA-COPD ('OCOS'). ...Expert commentary: As a consequence of COPD overlap syndromes, a transitio …
This is coined asthma-COPD overlap syndrome ('ACOS'). Other examples of such overlapping clinical states include bronchiectasis-COPD …
The trisomy 18 syndrome.
Cereda A, Carey JC. Cereda A, et al. Orphanet J Rare Dis. 2012 Oct 23;7:81. doi: 10.1186/1750-1172-7-81. Orphanet J Rare Dis. 2012. PMID: 23088440 Free PMC article. Review.
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chromosome 18, either full, mosaic trisomy, or partial trisomy 18q. The condition is the second most common autosomal trisomy syndrome af …
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chro …
Hemangioma-related syndromes.
Valdebran M, Wine Lee L. Valdebran M, et al. Curr Opin Pediatr. 2020 Aug;32(4):498-505. doi: 10.1097/MOP.0000000000000925. Curr Opin Pediatr. 2020. PMID: 32692048 Review.
The current review will discuss recent clinical advances in syndromes associated with segmental hemangiomas, including PHACE and LUMBAR syndrome. ...Segmental hemangiomas of the head and neck region may indicate a risk of PHACE syndrome and associated develop …
The current review will discuss recent clinical advances in syndromes associated with segmental hemangiomas, including PHACE and LUMB …
Neurovascular Syndromes.
Keith KA, Reed LK, Nguyen A, Qaiser R. Keith KA, et al. Neurosurg Clin N Am. 2022 Jan;33(1):135-148. doi: 10.1016/j.nec.2021.09.010. Neurosurg Clin N Am. 2022. PMID: 34801137 Review.
Patients with cerebrovascular syndromes are at risk for additional concerns associated with their syndrome. ...Precise diagnosis and appreciation for the underlying syndrome is critical for effective cerebrovascular and broader care. ...
Patients with cerebrovascular syndromes are at risk for additional concerns associated with their syndrome. ...Precise diagnos …
Syndromic Hydrocephalus.
Varagur K, Sanka SA, Strahle JM. Varagur K, et al. Neurosurg Clin N Am. 2022 Jan;33(1):67-79. doi: 10.1016/j.nec.2021.09.006. Neurosurg Clin N Am. 2022. PMID: 34801143 Free PMC article. Review.
Hydrocephalus, the abnormal accumulation and impaired circulation/clearance of cerebrospinal fluid, occurs as a common phenotypic feature of a diverse group of genetic syndromes. In this review, we outline the genetic mutations, pathogenesis, and accompanying symptoms unde …
Hydrocephalus, the abnormal accumulation and impaired circulation/clearance of cerebrospinal fluid, occurs as a common phenotypic feature of …
Renal-skin syndromes.
Has C, He Y. Has C, et al. Cell Tissue Res. 2017 Jul;369(1):63-73. doi: 10.1007/s00441-017-2623-y. Epub 2017 Apr 22. Cell Tissue Res. 2017. PMID: 28432467 Review.
Renal-skin syndroms are a group of genetic disorders with renal and cutaneous manifestations that target molecular components present in both organs. Inherited renal-skin syndromes are mainly associated with defects of cell-matrix adhesion. ...
Renal-skin syndroms are a group of genetic disorders with renal and cutaneous manifestations that target molecular components present …
Craniosynostosis: Neonatal Perspectives.
Bautista G. Bautista G. Neoreviews. 2021 Apr;22(4):e250-e257. doi: 10.1542/neo.22-4-e250. Neoreviews. 2021. PMID: 33795400
Multisuture synostoses are typically associated with distinct craniofacial syndromes, including Muenke syndrome, Apert syndrome, Crouzon syndrome, and Pfeiffer syndrome, and are thus categorized under syndromic craniosynostoses. ...
Multisuture synostoses are typically associated with distinct craniofacial syndromes, including Muenke syndrome, Apert synd …
Management of Ventricular Arrhythmias Worldwide: Comparison of the Latest ESC, AHA/ACC/HRS, and CCS/CHRS Guidelines.
Könemann H, Ellermann C, Zeppenfeld K, Eckardt L. Könemann H, et al. JACC Clin Electrophysiol. 2023 May;9(5):715-728. doi: 10.1016/j.jacep.2022.12.008. Epub 2023 Feb 22. JACC Clin Electrophysiol. 2023. PMID: 37225314 Review.
Overall, the recent ESC guideline places a greater emphasis on the value of cardiac magnetic resonance, genetic testing in cardiomyopathies and arrhythmia syndromes, and the use of risk calculators for risk stratification. Further significant differences can be found regar …
Overall, the recent ESC guideline places a greater emphasis on the value of cardiac magnetic resonance, genetic testing in cardiomyopathies …
Autoinflammatory syndromes.
Meier-Schiesser B, French LE. Meier-Schiesser B, et al. J Dtsch Dermatol Ges. 2021 Mar;19(3):400-426. doi: 10.1111/ddg.14332. Epub 2021 Feb 23. J Dtsch Dermatol Ges. 2021. PMID: 33620111
Autoinflammatory syndromes are a steadily growing group of inflammatory diseases caused by abnormal regulations of the innate immune system. ...
Autoinflammatory syndromes are a steadily growing group of inflammatory diseases caused by abnormal regulations of the innate immune …
Defining RASopathy.
Rauen KA. Rauen KA. Dis Model Mech. 2022 Feb 1;15(2):dmm049344. doi: 10.1242/dmm.049344. Epub 2022 Feb 1. Dis Model Mech. 2022. PMID: 35103797 Free PMC article.
The term RASopathy was originally created to describe a phenotypically similar group of medical genetic syndromes caused by germline pathogenic variants in components of the RAS/mitogen-activated protein kinase (RAS/MAPK) pathway. In defining a RASopathy syndrome, o …
The term RASopathy was originally created to describe a phenotypically similar group of medical genetic syndromes caused by germline …
407,800 results
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