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

Year Number of Results
1980 1
1982 2
1984 1
1989 2
1990 2
1991 2
1993 2
1994 2
1995 2
1997 5
1998 4
2000 4
2001 5
2002 4
2003 5
2004 5
2005 2
2006 6
2007 4
2008 5
2009 5
2010 5
2011 9
2012 8
2013 5
2014 7
2015 7
2016 13
2017 12
2018 7
2019 10
2020 17
2021 17
2022 21
2023 16
2024 4

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199 results

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Page 1
Juvenile Idiopathic Arthritis.
Barut K, Adrovic A, Şahin S, Kasapçopur Ö. Barut K, et al. Balkan Med J. 2017 Apr 5;34(2):90-101. doi: 10.4274/balkanmedj.2017.0111. Balkan Med J. 2017. PMID: 28418334 Free PMC article.
The disease is divided into several subgroups, according to demographic characteristics, clinical features, treatment modalities and disease prognosis. Systemic juvenile idiopathic arthritis, which is one of the most frequent disease subtypes, is characterized by recurrent …
The disease is divided into several subgroups, according to demographic characteristics, clinical features, treatment modalities and disease …
Sacral Dimple.
Khairy S, Azzubi M. Khairy S, et al. World Neurosurg. 2017 May;101:811.e7-811.e8. doi: 10.1016/j.wneu.2017.02.074. Epub 2017 Feb 27. World Neurosurg. 2017. PMID: 28245993
He tolerated the procedure well, and his weakness improved. The antibiotic course was completed, and the external ventricular drain was removed. ...
He tolerated the procedure well, and his weakness improved. The antibiotic course was completed, and the external ventricular drain w …
ROSAH syndrome mimicking chronic uveitis.
Fardeau C, Alafaleq M, Dhaenens CM, Dollfus H, Koné-Paut I, Grunewald O, Morel JB, Titah C, Saadoun D, Lazeran PO, Meunier I. Fardeau C, et al. Clin Genet. 2023 Apr;103(4):453-458. doi: 10.1111/cge.14286. Epub 2022 Dec 30. Clin Genet. 2023. PMID: 36543582
Gain-of-function mutations in ALPK1 cause an NF-kappaB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Kozycki CT, Kodati S, Huryn L, Wang H, Warner BM, Jani P, Hammoud D, Abu-Asab MS, Jittayasothorn Y, Mattapallil MJ, Tsai WL, Ullah E, Zhou P, Tian X, Soldatos A, Moutsopoulos N, Kao-Hsieh M, Heller T, Cowen EW, Lee CR, Toro C, Kalsi S, Khavandgar Z, Baer A, Beach M, Long Priel D, Nehrebecky M, Rosenzweig S, Romeo T, Deuitch N, Brenchley L, Pelayo E, Zein W, Sen N, Yang AH, Farley G, Sweetser DA, Briere L, Yang J, de Oliveira Poswar F, Schwartz IVD, Silva Alves T, Dusser P, Koné-Paut I, Touitou I, Titah SM, van Hagen PM, van Wijck RTA, van der Spek PJ, Yano H, Benneche A, Apalset EM, Jansson RW, Caspi RR, Kuhns DB, Gadina M, Takada H, Ida H, Nishikomori R, Verrecchia E, Sangiorgi E, Manna R, Brooks BP, Sobrin L, Hufnagel RB, Beck D, Shao F, Ombrello AK, Aksentijevich I, Kastner DL; Undiagnosed Diseases Network. Kozycki CT, et al. Ann Rheum Dis. 2022 Oct;81(10):1453-1464. doi: 10.1136/annrheumdis-2022-222629. Epub 2022 Jul 22. Ann Rheum Dis. 2022. PMID: 35868845 Free PMC article.
Role of glucocorticoids in Kawasaki disease.
Miura M. Miura M. Int J Rheum Dis. 2018 Jan;21(1):70-75. doi: 10.1111/1756-185X.13209. Epub 2017 Nov 3. Int J Rheum Dis. 2018. PMID: 29105310 Review.
A clinical trial known as the Randomized controlled trial to Assess Immunoglobulin plus Steroid Efficacy for KD (RAISE) Study, demonstrated the efficacy of prednisolone with initial IVIg, especially in predicted IVIg non-responders. Several meta-analyses have also supporte …
A clinical trial known as the Randomized controlled trial to Assess Immunoglobulin plus Steroid Efficacy for KD (RAISE) Study, demonstrated …
An early-onset SLE patient with a novel paternal inherited BACH2 mutation.
Zhou L, Sun G, Chen R, Chen J, Fang S, Xu Q, Tang W, Dai R, Zhang Z, An Y, Tang X, Zhao X. Zhou L, et al. J Clin Immunol. 2023 Aug;43(6):1367-1378. doi: 10.1007/s10875-023-01506-7. Epub 2023 May 6. J Clin Immunol. 2023. PMID: 37148421
Whole exome sequencing analysis of the patient and her parents revealed a novel heterozygous point mutation in BACH2, c.G1727T, resulting in substitution of a highly conserved arginine with leucine (R576L), which is predicted to be deleterious, in the patient and her fathe …
Whole exome sequencing analysis of the patient and her parents revealed a novel heterozygous point mutation in BACH2, c.G1727T, resulting in …
Schnitzler's syndrome: diagnosis, treatment, and follow-up.
Simon A, Asli B, Braun-Falco M, De Koning H, Fermand JP, Grattan C, Krause K, Lachmann H, Lenormand C, Martinez-Taboada V, Maurer M, Peters M, Rizzi R, Rongioletti F, Ruzicka T, Schnitzler L, Schubert B, Sibilia J, Lipsker D. Simon A, et al. Allergy. 2013;68(5):562-8. doi: 10.1111/all.12129. Epub 2013 Mar 9. Allergy. 2013. PMID: 23480774 Review.
Approach to recurrent fever in childhood.
Soon GS, Laxer RM. Soon GS, et al. Can Fam Physician. 2017 Oct;63(10):756-762. Can Fam Physician. 2017. PMID: 29025800 Free PMC article. Review.
SOURCES OF INFORMATION: PubMed was searched for relevant articles regarding the pathogenesis, clinical findings, diagnosis, prognosis, and treatment of periodic fever and autoinflammatory syndromes. ...
SOURCES OF INFORMATION: PubMed was searched for relevant articles regarding the pathogenesis, clinical findings, diagnosis, prognosis …
Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome: main features and an algorithm for clinical practice.
Batu ED. Batu ED. Rheumatol Int. 2019 Jun;39(6):957-970. doi: 10.1007/s00296-019-04257-0. Epub 2019 Feb 23. Rheumatol Int. 2019. PMID: 30798384 Review.
The main topics covered are the epidemiology, clinical manifestations, diagnosis, differential diagnosis, etiopathogenesis, genetics, management, disease course and prognosis, disease in adults, unsolved issues, and unmet needs in PFAPA. ...There remain unsolved iss …
The main topics covered are the epidemiology, clinical manifestations, diagnosis, differential diagnosis, etiopathogenesis, genetics, manage …
Clinical and Genetic Characteristics of BCG Disease in Chinese Children: a Retrospective Study.
Zeng Y, Ying W, Wang W, Hou J, Liu L, Sun B, Hui X, Gu Y, Song X, Wang X, Sun J. Zeng Y, et al. J Clin Immunol. 2023 May;43(4):756-768. doi: 10.1007/s10875-022-01422-2. Epub 2023 Jan 20. J Clin Immunol. 2023. PMID: 36662455
The MSMD group had the highest probability of disseminated infection (48.3%). The course of anti-tuberculosis treatment and the survival time between patients with PID and without identified genetic etiology were similar. ...
The MSMD group had the highest probability of disseminated infection (48.3%). The course of anti-tuberculosis treatment and the survi …
199 results