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

Year Number of Results
1957 1
1976 1
1977 1
1980 4
1981 1
1982 1
1983 2
1984 1
1985 3
1986 3
1987 4
1988 2
1989 6
1990 8
1991 5
1992 5
1993 7
1994 7
1995 6
1996 11
1997 11
1998 9
1999 18
2000 26
2001 23
2002 18
2003 19
2004 29
2005 27
2006 36
2007 26
2008 37
2009 36
2010 32
2011 38
2012 45
2013 54
2014 51
2015 62
2016 41
2017 54
2018 48
2019 56
2020 64
2021 72
2022 44
2023 52
2024 20

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Search Results

995 results

Results by year

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Page 1
Achalasia.
Savarino E, Bhatia S, Roman S, Sifrim D, Tack J, Thompson SK, Gyawali CP. Savarino E, et al. Nat Rev Dis Primers. 2022 May 5;8(1):28. doi: 10.1038/s41572-022-00356-8. Nat Rev Dis Primers. 2022. PMID: 35513420 Review.
Achalasia is a rare disorder of the oesophageal smooth muscle characterized by impaired relaxation of the lower oesophageal sphincter (LES) and absent or spastic contractions in the oesophageal body. ...Although symptom questionnaires are not useful for diagnosis, t …
Achalasia is a rare disorder of the oesophageal smooth muscle characterized by impaired relaxation of the lower oesophageal sp …
Stiff person syndrome.
Hadavi S, Noyce AJ, Leslie RD, Giovannoni G. Hadavi S, et al. Pract Neurol. 2011 Oct;11(5):272-82. doi: 10.1136/practneurol-2011-000071. Pract Neurol. 2011. PMID: 21921002 Review.
Stiff person syndrome (SPS) is a rare disorder, characterised by fluctuating rigidity and stiffness of the axial and proximal lower limb muscles, with superimposed painful spasms and continuous motor unit activity on electromyography. Although rare in general neurol …
Stiff person syndrome (SPS) is a rare disorder, characterised by fluctuating rigidity and stiffness of the axial and proximal …
Pathophysiology, Diagnosis, and Management of Chronic Intestinal Pseudo-Obstruction.
Downes TJ, Cheruvu MS, Karunaratne TB, De Giorgio R, Farmer AD. Downes TJ, et al. J Clin Gastroenterol. 2018 Jul;52(6):477-489. doi: 10.1097/MCG.0000000000001047. J Clin Gastroenterol. 2018. PMID: 29877952 Review.
Chronic intestinal pseudo-obstruction (CIPO) is a rare disorder characterized by an impairment of coordinated propulsive activity in the gastrointestinal (GI) tract, which clinically mimics mechanical intestinal obstruction. ...
Chronic intestinal pseudo-obstruction (CIPO) is a rare disorder characterized by an impairment of coordinated propulsive activ …
Lipoprotein glomerulopathy.
Tsimihodimos V, Elisaf M. Tsimihodimos V, et al. Curr Opin Lipidol. 2011 Aug;22(4):262-9. doi: 10.1097/MOL.0b013e328345ebb0. Curr Opin Lipidol. 2011. PMID: 21464714 Review.
PURPOSE OF REVIEW: Lipoprotein glomerulopathy is a rare disorder characterized by proteinuria, renal insufficiency and disturbances in lipoprotein metabolism closely related to those observed in type III hyperlipidemia. ...
PURPOSE OF REVIEW: Lipoprotein glomerulopathy is a rare disorder characterized by proteinuria, renal insufficiency and disturb …
Congenital Hyperinsulinism.
Minakova E, Chu A. Minakova E, et al. Pediatr Ann. 2017 Nov 1;46(11):e409-e414. doi: 10.3928/19382359-20171020-01. Pediatr Ann. 2017. PMID: 29131920
Congenital hyperinsulinism is a rare disorder that commonly presents in the immediate postnatal period as persistent hypoglycemia. The condition is frequently resistant to medical therapies, and the genetic mutations implicated in the disorder can be predictive …
Congenital hyperinsulinism is a rare disorder that commonly presents in the immediate postnatal period as persistent hypoglyce …
Cryofibrinogenemia: What Rheumatologists Should Know.
Santiago MB, Melo BS. Santiago MB, et al. Curr Rheumatol Rev. 2022;18(3):186-194. doi: 10.2174/1573397118666220325110737. Curr Rheumatol Rev. 2022. PMID: 35339184 Review.
This protein has the property of precipitating at lower temperatures. Cryofibrinogenemia is a rare disorder, clinically characterized by skin lesions, such as ulcers, necrosis, livedo reticularis, arthralgia, thrombosis, and limb ischemia. These features are most of …
This protein has the property of precipitating at lower temperatures. Cryofibrinogenemia is a rare disorder, clinically charac …
Single-organ vasculitis.
Hernández-Rodríguez J, Molloy ES, Hoffman GS. Hernández-Rodríguez J, et al. Curr Opin Rheumatol. 2008 Jan;20(1):40-6. doi: 10.1097/BOR.0b013e3282f176a0. Curr Opin Rheumatol. 2008. PMID: 18281856 Review.
PURPOSE OF REVIEW: To provide a critical analysis of a rare disorder, single-organ vasculitis, emphasizing those organs in which the excision of the vasculitic lesion can be curative. ...Depending on the organ affected, some clinical, serological and histopathologic …
PURPOSE OF REVIEW: To provide a critical analysis of a rare disorder, single-organ vasculitis, emphasizing those organs in whi …
Dyskeratosis congenita.
Keeling B, Antia C, Steadmon M, Wesson S, Williams C. Keeling B, et al. Dermatol Online J. 2014 Sep 16;20(9):13030/qt2k99x2kq. Dermatol Online J. 2014. PMID: 25244172
IMPORTANCE: Dyskeratosis congenita is a rare disorder that often leads to early death owing to a variety of complications and associated disorders. Early diagnosis and intervention is important in care for patients affected by this disease. OBSERVATIONS: We d …
IMPORTANCE: Dyskeratosis congenita is a rare disorder that often leads to early death owing to a variety of complications and …
Dystonia-plus syndromes.
Asmus F, Gasser T. Asmus F, et al. Eur J Neurol. 2010 Jul;17 Suppl 1:37-45. doi: 10.1111/j.1468-1331.2010.03049.x. Eur J Neurol. 2010. PMID: 20590807 Review.
The combination of dystonia and parkinsonism can only be rarely observed in non-degenerative syndromes. Besides DRD, two additional syndromes have been classified. Rapid-onset dystonia-parkinsonism (RPD, DYT12) is a rare disorder with an abrupt onset of sympt …
The combination of dystonia and parkinsonism can only be rarely observed in non-degenerative syndromes. Besides DRD, two additional s …
Yellow nail syndrome: a review.
Vignes S, Baran R. Vignes S, et al. Orphanet J Rare Dis. 2017 Feb 27;12(1):42. doi: 10.1186/s13023-017-0594-4. Orphanet J Rare Dis. 2017. PMID: 28241848 Free PMC article. Review.
Yellow nail syndrome (YNS; OMIM 153300, ORPHA662) is a very rare disorder that almost always occurs after 50 years of age but a juvenile or familial form has also been observed. ...
Yellow nail syndrome (YNS; OMIM 153300, ORPHA662) is a very rare disorder that almost always occurs after 50 years of age but …
995 results