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

Year Number of Results
1972 1
1975 4
1978 4
1979 1
1980 2
1981 1
1982 5
1983 5
1984 11
1985 6
1986 7
1987 11
1988 30
1989 33
1990 29
1991 43
1992 37
1993 52
1994 42
1995 43
1996 40
1997 43
1998 52
1999 63
2000 46
2001 62
2002 63
2003 65
2004 71
2005 84
2006 88
2007 82
2008 90
2009 80
2010 86
2011 101
2012 105
2013 110
2014 113
2015 102
2016 93
2017 108
2018 108
2019 114
2020 141
2021 147
2022 137
2023 123
2024 35

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2,654 results

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The following term was not found in PubMed: glabella-microcephaly-hypogenitalism
Page 1
Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations.
Dinarvand P, Davaro EP, Doan JV, Ising ME, Evans NR, Phillips NJ, Lai J, Guzman MA. Dinarvand P, et al. Arch Pathol Lab Med. 2019 Nov;143(11):1382-1398. doi: 10.5858/arpa.2018-0570-RA. Epub 2019 May 9. Arch Pathol Lab Med. 2019. PMID: 31070935 Free article. Review.
These manifestations have historically been subcategorized as Gardner syndrome, Turcot syndrome, or gastric adenocarcinoma and proximal polyposis of the stomach. Recent studies, however, correlate the severity of gastrointestinal disease and the prominence of …
These manifestations have historically been subcategorized as Gardner syndrome, Turcot syndrome, or gastric adenocarcinoma and …
Epilepsy Overview and Revised Classification of Seizures and Epilepsies.
Pack AM. Pack AM. Continuum (Minneap Minn). 2019 Apr;25(2):306-321. doi: 10.1212/CON.0000000000000707. Continuum (Minneap Minn). 2019. PMID: 30921011 Review.
PURPOSE OF REVIEW: The classification of seizures, epilepsies, and epilepsy syndromes creates a framework for clinicians, researchers, and patients and their families. ...Focal seizures are classified according to the individual's level of awareness, the most prominent …
PURPOSE OF REVIEW: The classification of seizures, epilepsies, and epilepsy syndromes creates a framework for clinicians, researchers …
Update of New Daily Persistent Headache.
Peng KP, Wang SJ. Peng KP, et al. Curr Pain Headache Rep. 2022 Jan;26(1):79-84. doi: 10.1007/s11916-022-01005-1. Epub 2022 Jan 25. Curr Pain Headache Rep. 2022. PMID: 35076874 Free PMC article. Review.
The association with both cephalic and extracephalic pathologies suggests that NDPH is rather a syndrome with more than one disease mechanism. Recent clinical studies confirmed that migrainous headache remained the most prominent phenotype of NDPH, echoing the chang …
The association with both cephalic and extracephalic pathologies suggests that NDPH is rather a syndrome with more than one disease m …
Mycoplasma pneumoniae-induced rash and mucositis as a syndrome distinct from Stevens-Johnson syndrome and erythema multiforme: a systematic review.
Canavan TN, Mathes EF, Frieden I, Shinkai K. Canavan TN, et al. J Am Acad Dermatol. 2015 Feb;72(2):239-45. doi: 10.1016/j.jaad.2014.06.026. J Am Acad Dermatol. 2015. PMID: 25592340 Review.
These eruptions, which have been termed either "Stevens-Johnson syndrome" or "erythema multiforme" in the literature, may differ from drug-induced Stevens-Johnson syndrome or viral-associated erythema multiforme. ...CONCLUSION: M pneumoniae-associated mucocutaneous …
These eruptions, which have been termed either "Stevens-Johnson syndrome" or "erythema multiforme" in the literature, may differ from …
Eosinophilic granulomatosis with polyangiitis: understanding the disease and its management.
Trivioli G, Terrier B, Vaglio A. Trivioli G, et al. Rheumatology (Oxford). 2020 May 1;59(Suppl 3):iii84-iii94. doi: 10.1093/rheumatology/kez570. Rheumatology (Oxford). 2020. PMID: 32348510 Review.
The clinical presentation is variable, but two main clinic-pathologic subsets can be distinguished: one hallmarked by positive ANCA and predominant 'vasculitic' manifestations (e.g. glomerulonephritis, purpura and mononeuritis multiplex) and the other by negative ANCA and prom …
The clinical presentation is variable, but two main clinic-pathologic subsets can be distinguished: one hallmarked by positive ANCA and pred …
Forty Years of Molecular Diagnostics for Infectious Diseases.
Schmitz JE, Stratton CW, Persing DH, Tang YW. Schmitz JE, et al. J Clin Microbiol. 2022 Oct 19;60(10):e0244621. doi: 10.1128/jcm.02446-21. Epub 2022 Jul 19. J Clin Microbiol. 2022. PMID: 35852340 Free PMC article. Review.
In this context, we review broadly the progression of molecular techniques in clinical microbiology, to their current prominence. Notably, these methods now entail both the detection and quantification of microbial nucleic acids, along with their sequence-based characteriz …
In this context, we review broadly the progression of molecular techniques in clinical microbiology, to their current prominence. Not …
Movement disorders with neuronal antibodies: syndromic approach, genetic parallels and pathophysiology.
Balint B, Vincent A, Meinck HM, Irani SR, Bhatia KP. Balint B, et al. Brain. 2018 Jan 1;141(1):13-36. doi: 10.1093/brain/awx189. Brain. 2018. PMID: 29053777 Free PMC article. Review.
Movement disorders are a prominent and common feature in many autoantibody-associated neurological diseases, a group of potentially treatable conditions that can mimic infectious, metabolic or neurodegenerative disease. ...In this review, we first describe the antibodies a …
Movement disorders are a prominent and common feature in many autoantibody-associated neurological diseases, a group of potentially t …
The diagnosis of multiple sclerosis and the various related demyelinating syndromes: a critical review.
Karussis D. Karussis D. J Autoimmun. 2014 Feb-Mar;48-49:134-42. doi: 10.1016/j.jaut.2014.01.022. Epub 2014 Feb 10. J Autoimmun. 2014. PMID: 24524923 Review.
MS is one of the most common causes of neurological disability in young adults. Several variants of MS (and CNS demyelinating syndromes in general) have been nowadays defined in an effort to increase the diagnostic accuracy, to identify the unique immunopathogenic profile …
MS is one of the most common causes of neurological disability in young adults. Several variants of MS (and CNS demyelinating syndromes …
Autoimmune Neurogenic Dysphagia.
Stathopoulos P, Dalakas MC. Stathopoulos P, et al. Dysphagia. 2022 Jun;37(3):473-487. doi: 10.1007/s00455-021-10338-9. Epub 2021 Jul 5. Dysphagia. 2022. PMID: 34226958 Free PMC article. Review.
Acute-onset dysphagia is often seen in Guillain-Barre syndrome variants and slowly progressive dysphagia in paraneoplastic neuropathies highlighted by the presence of specific autoantibodies. ...Less common, but often overlooked, is dysphagia in stiff-person syndrome …
Acute-onset dysphagia is often seen in Guillain-Barre syndrome variants and slowly progressive dysphagia in paraneoplastic neuropathi …
Neuroacanthocytosis.
Walker RH, Jung HH, Danek A. Walker RH, et al. Handb Clin Neurol. 2011;100:141-51. doi: 10.1016/B978-0-444-52014-2.00007-0. Handb Clin Neurol. 2011. PMID: 21496574 Review.
Psychiatric and cognitive symptoms may be prominent. There can be considerable phenotypic overlap; however, features of inheritance, age of onset, neuroimaging and laboratory findings, in addition to the spectrum of central and peripheral neurological abnormalities and ext …
Psychiatric and cognitive symptoms may be prominent. There can be considerable phenotypic overlap; however, features of inheritance, …
2,654 results