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Year Number of Results
1976 2
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1992 5
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1999 11
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865 results

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Quoted phrase not found in phrase index: "Rare insulin-resistance syndrome"
Page 1
Insulin pharmacokinetics.
Binder C, Lauritzen T, Faber O, Pramming S. Binder C, et al. Diabetes Care. 1984 Mar-Apr;7(2):188-99. doi: 10.2337/diacare.7.2.188. Diabetes Care. 1984. PMID: 6376015 Review.
The distribution and metabolism of absorbed insulin follow that of endogenous insulin. The distribution and metabolism cannot be actively changed, except in the case of circulating insulin antibodies, which in rare cases also may cause insulin …
The distribution and metabolism of absorbed insulin follow that of endogenous insulin. The distribution and metabolism cannot …
Causes, consequences, and treatment of metabolically unhealthy fat distribution.
Stefan N. Stefan N. Lancet Diabetes Endocrinol. 2020 Jul;8(7):616-627. doi: 10.1016/S2213-8587(20)30110-8. Lancet Diabetes Endocrinol. 2020. PMID: 32559477 Review.
However, for a given fat mass, there is a large variability in the risk prediction of these cardiometabolic diseases. For example, some lean people unexpectedly have a risk of type 2 diabetes and cardiovascular disease that is similar to the increased risk that is observed …
However, for a given fat mass, there is a large variability in the risk prediction of these cardiometabolic diseases. For example, so …
Critical care hepatology: definitions, incidence, prognosis and role of liver failure in critically ill patients.
Perez Ruiz de Garibay A, Kortgen A, Leonhardt J, Zipprich A, Bauer M. Perez Ruiz de Garibay A, et al. Crit Care. 2022 Sep 26;26(1):289. doi: 10.1186/s13054-022-04163-1. Crit Care. 2022. PMID: 36163253 Free PMC article. Review.
Dysfunction of the liver in general reflects a critical event in "Multiple Organ Dysfunction Syndrome" due to immunologic, regulatory and metabolic functions of liver parenchymal and non-parenchymal cells. ...In the present work, we review the different definitions …
Dysfunction of the liver in general reflects a critical event in "Multiple Organ Dysfunction Syndrome" due to immunologic, regulatory …
Rhabdomyolysis: an evaluation of 475 hospitalized patients.
Melli G, Chaudhry V, Cornblath DR. Melli G, et al. Medicine (Baltimore). 2005 Nov;84(6):377-385. doi: 10.1097/01.md.0000188565.48918.41. Medicine (Baltimore). 2005. PMID: 16267412 Free article.
Rhabdomyolysis is a common and potentially lethal clinical syndrome that results from acute muscle fiber necrosis with leakage of muscle constituents into blood. ...The absence of urine myoglobin, by qualitative assay, does not exclude rhabdomyolysis. With appropriate care …
Rhabdomyolysis is a common and potentially lethal clinical syndrome that results from acute muscle fiber necrosis with leakage of mus …
Triglyceride-glucose index and coronary artery disease: a systematic review and meta-analysis of risk, severity, and prognosis.
Liang S, Wang C, Zhang J, Liu Z, Bai Y, Chen Z, Huang H, He Y. Liang S, et al. Cardiovasc Diabetol. 2023 Jul 6;22(1):170. doi: 10.1186/s12933-023-01906-4. Cardiovasc Diabetol. 2023. PMID: 37415168 Free PMC article.
BACKGROUND: The TyG index is an indicator of insulin resistance (IR), which is associated with the development and prognosis of cardiovascular disease. ...CONCLUSIONS: The TyG index is a simple new synthetic index that has been proven to be a valuable tool in …
BACKGROUND: The TyG index is an indicator of insulin resistance (IR), which is associated with the development and prognosi …
Childhood-onset Craniopharyngioma.
Otte A, Müller HL. Otte A, et al. J Clin Endocrinol Metab. 2021 Sep 27;106(10):e3820-e3836. doi: 10.1210/clinem/dgab397. J Clin Endocrinol Metab. 2021. PMID: 34086900 Review.
Craniopharyngiomas are rare embryonic malformational tumors of the sellar/parasellar region, classified by the World Health Organization (WHO) as tumors with low-grade malignancy (WHO I). ...Severe impairment of quality of life and comorbidities such as metabolic …
Craniopharyngiomas are rare embryonic malformational tumors of the sellar/parasellar region, classified by the World Health Organizat …
Revesz syndrome revisited.
Karremann M, Neumaier-Probst E, Schlichtenbrede F, Beier F, Brümmendorf TH, Cremer FW, Bader P, Dürken M. Karremann M, et al. Orphanet J Rare Dis. 2020 Oct 23;15(1):299. doi: 10.1186/s13023-020-01553-y. Orphanet J Rare Dis. 2020. PMID: 33097095 Free PMC article. Review.
BACKGROUND: Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in the literature. ...Survival is dismal, but stem cell transplantation may be performed successfully and might improve prognosis in the …
BACKGROUND: Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in t …
Antiphospholipid-related chorea.
Farag M, Hunt BJ, Andrews TC. Farag M, et al. Pract Neurol. 2023 Apr;23(2):150-152. doi: 10.1136/pn-2022-003587. Epub 2022 Oct 7. Pract Neurol. 2023. PMID: 36207127
Chorea is a rare neurological manifestation of antiphospholipid syndrome. The pathophysiological mechanisms underlying aPL-related chorea are still debated. ...Here, we report a patient with isolated aPL-related chorea that followed a relapsing-remitting course …
Chorea is a rare neurological manifestation of antiphospholipid syndrome. The pathophysiological mechanisms underlying aPL-rel …
The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Martinelli D, Diodato D, Ponzi E, Monné M, Boenzi S, Bertini E, Fiermonte G, Dionisi-Vici C. Martinelli D, et al. Orphanet J Rare Dis. 2015 Mar 11;10:29. doi: 10.1186/s13023-015-0242-9. Orphanet J Rare Dis. 2015. PMID: 25874378 Free PMC article. Review.
BACKGROUND: Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare autosomal recessive disorder of the urea cycle. ...CONCLUSIONS: This paper provides detailed information on the clinical, metabolic and genetic profiles of all HHH synd …
BACKGROUND: Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare autosomal recessive disorder of the ur …
Locked-in syndrome.
Cardwell MS. Cardwell MS. Tex Med. 2013 Feb 1;109(2):e1. Tex Med. 2013. PMID: 23378122
Locked-in syndrome is a rare neuropsychological disorder. Its primary features are quadriplegia and paralysis of the cranial nerves except for those responsible for vertical eye movements. ...The clinical manifestations, differential diagnosis, neuropsychological as …
Locked-in syndrome is a rare neuropsychological disorder. Its primary features are quadriplegia and paralysis of the cranial n …
865 results