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

Year Number of Results
1923 1
1949 1
1950 1
1952 3
1953 4
1954 2
1955 2
1956 2
1957 1
1959 1
1960 4
1961 1
1962 2
1963 6
1964 4
1965 1
1966 6
1967 13
1968 10
1969 13
1970 10
1971 14
1972 18
1973 20
1974 16
1975 41
1976 58
1977 57
1978 57
1979 62
1980 67
1981 68
1982 79
1983 68
1984 77
1985 67
1986 83
1987 75
1988 95
1989 106
1990 128
1991 125
1992 103
1993 133
1994 125
1995 137
1996 118
1997 107
1998 102
1999 131
2000 118
2001 115
2002 111
2003 112
2004 116
2005 117
2006 138
2007 149
2008 156
2009 151
2010 159
2011 177
2012 197
2013 231
2014 217
2015 273
2016 255
2017 212
2018 224
2019 251
2020 296
2021 291
2022 299
2023 283
2024 100

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6,577 results

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Page 1
New insights into the pathophysiology of methylmalonic acidemia.
Head PE, Meier JL, Venditti CP. Head PE, et al. J Inherit Metab Dis. 2023 May;46(3):436-449. doi: 10.1002/jimd.12617. J Inherit Metab Dis. 2023. PMID: 37078237 Free PMC article. Review.
Methylmalonic acidemia (MMA) is a severe inborn error of metabolism that is characterized by pleiotropic metabolic perturbations and multiorgan pathology. ...Therefore, targeting posttranslational modifications may represent a new therapeutic approach to treat MMA and rela …
Methylmalonic acidemia (MMA) is a severe inborn error of metabolism that is characterized by pleiotropic metabolic perturbations and …
Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision.
Forny P, Hörster F, Ballhausen D, Chakrapani A, Chapman KA, Dionisi-Vici C, Dixon M, Grünert SC, Grunewald S, Haliloglu G, Hochuli M, Honzik T, Karall D, Martinelli D, Molema F, Sass JO, Scholl-Bürgi S, Tal G, Williams M, Huemer M, Baumgartner MR. Forny P, et al. J Inherit Metab Dis. 2021 May;44(3):566-592. doi: 10.1002/jimd.12370. Epub 2021 Mar 9. J Inherit Metab Dis. 2021. PMID: 33595124 Free PMC article.
Isolated methylmalonic acidaemia (MMA) and propionic acidaemia (PA) are rare inherited metabolic diseases. ...
Isolated methylmalonic acidaemia (MMA) and propionic acidaemia (PA) are rare inherited metabolic diseases. ...
β-hydroxybutyrate inhibits ferroptosis-mediated pancreatic damage in acute liver failure through the increase of H3K9bhb.
Zheng Y, Sun W, Shan C, Li B, Liu J, Xing H, Xu Q, Cui B, Zhu W, Chen J, Liu L, Yang T, Sun N, Li X. Zheng Y, et al. Cell Rep. 2022 Dec 20;41(12):111847. doi: 10.1016/j.celrep.2022.111847. Cell Rep. 2022. PMID: 36543135 Free article.
Acute pancreatitis and hyperamylasemia are often seen in patients with acute liver failure (ALF). ...The analysis of 1,264 clinical cases of liver failure (LF) showed that the incidence of hyperamylasemia and hyperlipasemia in patients with LF is 5.5% and 20%, respe …
Acute pancreatitis and hyperamylasemia are often seen in patients with acute liver failure (ALF). ...The analysis of 1,264 clinical c …
Postpancreatectomy Acute Pancreatitis (PPAP): Definition and Grading From the International Study Group for Pancreatic Surgery (ISGPS).
Marchegiani G, Barreto SG, Bannone E, Sarr M, Vollmer CM, Connor S, Falconi M, Besselink MG, Salvia R, Wolfgang CL, Zyromski NJ, Yeo CJ, Adham M, Siriwardena AK, Takaori K, Hilal MA, Loos M, Probst P, Hackert T, Strobel O, Busch ORC, Lillemoe KD, Miao Y, Halloran CM, Werner J, Friess H, Izbicki JR, Bockhorn M, Vashist YK, Conlon K, Passas I, Gianotti L, Del Chiaro M, Schulick RD, Montorsi M, Oláh A, Fusai GK, Serrablo A, Zerbi A, Fingerhut A, Andersson R, Padbury R, Dervenis C, Neoptolemos JP, Bassi C, Büchler MW, Shrikhande SV; International Study Group for Pancreatic Surgery. Marchegiani G, et al. Ann Surg. 2022 Apr 1;275(4):663-672. doi: 10.1097/SLA.0000000000005226. Ann Surg. 2022. PMID: 34596077
The diagnosis requires (1) a sustained postoperative serum hyperamylasemia (POH) greater than the institutional upper limit of normal for at least the first 48 hours postoperatively, (2) associated with clinically relevant features, and (3) radiologic alterations consisten …
The diagnosis requires (1) a sustained postoperative serum hyperamylasemia (POH) greater than the institutional upper limit of normal …
Acrodermatitis acidaemica.
Maguire CA, Chong H, Ramachandran R, Popoola J, Akhras V, Singh M. Maguire CA, et al. Clin Exp Dermatol. 2018 Apr;43(3):315-318. doi: 10.1111/ced.13369. Epub 2018 Jan 15. Clin Exp Dermatol. 2018. PMID: 29336047
Methylmalonic acidaemia (MMA) is an inborn error of amino acid metabolism that may be associated with cutaneous manifestations mimicking other diagnoses, including staphylococcal scalded skin syndrome (SSSS), psoriasis and acrodermatitis enteropathica. ...
Methylmalonic acidaemia (MMA) is an inborn error of amino acid metabolism that may be associated with cutaneous manifestations mimick …
Amylase.
Reynolds TM. Reynolds TM. Br J Hosp Med (Lond). 2009 Jan;70(1):M8-9. doi: 10.12968/hmed.2009.70.Sup1.37706. Br J Hosp Med (Lond). 2009. PMID: 19357566 No abstract available.
Effects of Somatostatin and Indomethacin Mono or Combination Therapy on High-risk Hyperamylasemia and Post-pancreatitis Endoscopic Retrograde Cholangiopancreatography Patients: A Randomized Study.
Wu Z, Xiao G, Wang G, Xiong L, Qiu P, Tan S. Wu Z, et al. Surg Laparosc Endosc Percutan Tech. 2023 Oct 1;33(5):474-479. doi: 10.1097/SLE.0000000000001202. Surg Laparosc Endosc Percutan Tech. 2023. PMID: 37523580 Free PMC article. Clinical Trial.
The pre operation and post operation (at 6, 12, and 24 h) hospitalization cost, length of stay, the occurrence of hyperamylasemia and PEP, levels of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), IL-8, and VAS pain score were determined in the 4 groups. ... …
The pre operation and post operation (at 6, 12, and 24 h) hospitalization cost, length of stay, the occurrence of hyperamylasemia and …
Malignancy-associated hyperamylasaemia.
Srivastava R, Murphy MJ, Fraser CG. Srivastava R, et al. Ann Clin Biochem. 2014 Sep;51(Pt 5):619. doi: 10.1177/0004563214531402. Epub 2014 Apr 24. Ann Clin Biochem. 2014. PMID: 24763853 No abstract available.
Challenges and strategies for clinical trials in propionic and methylmalonic acidemias.
Vockley J, Burton B, Jurecka A, Ganju J, Leiro B, Zori R, Longo N. Vockley J, et al. Mol Genet Metab. 2023 Jul;139(3):107612. doi: 10.1016/j.ymgme.2023.107612. Epub 2023 May 21. Mol Genet Metab. 2023. PMID: 37245378 Free article. Review.
Clinical trial development in rare diseases poses significant study design and methodology challenges, such as disease heterogeneity and appropriate patient selection, identification and selection of key endpoints, decisions on study duration, choice of control groups, selection …
Clinical trial development in rare diseases poses significant study design and methodology challenges, such as disease heterogeneity and app …
Biomarkers for drug development in propionic and methylmalonic acidemias.
Longo N, Sass JO, Jurecka A, Vockley J. Longo N, et al. J Inherit Metab Dis. 2022 Mar;45(2):132-143. doi: 10.1002/jimd.12478. Epub 2022 Jan 26. J Inherit Metab Dis. 2022. PMID: 35038174 Free PMC article. Review.
There is an unmet need for the development and validation of biomarkers and surrogate endpoints for clinical trials in propionic acidemia (PA) and methylmalonic acidemia (MMA). This review examines the pathophysiology and clinical consequences of PA and MMA that cou …
There is an unmet need for the development and validation of biomarkers and surrogate endpoints for clinical trials in propionic acidemia …
6,577 results