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

Year Number of Results
1983 1
1984 1
1986 1
1987 1
1991 2
1992 1
1993 1
1994 1
1995 2
1996 1
1997 1
1998 1
1999 1
2000 1
2001 2
2002 5
2003 2
2004 2
2005 6
2006 8
2007 5
2008 8
2009 5
2010 5
2011 1
2012 3
2013 8
2014 5
2015 2
2016 2
2017 4
2018 4
2019 3
2020 2
2021 1
2023 1
2024 0

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91 results

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Page 1
Type 3c (pancreatogenic) diabetes mellitus secondary to chronic pancreatitis and pancreatic cancer.
Hart PA, Bellin MD, Andersen DK, Bradley D, Cruz-Monserrate Z, Forsmark CE, Goodarzi MO, Habtezion A, Korc M, Kudva YC, Pandol SJ, Yadav D, Chari ST; Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer(CPDPC). Hart PA, et al. Lancet Gastroenterol Hepatol. 2016 Nov;1(3):226-237. doi: 10.1016/S2468-1253(16)30106-6. Epub 2016 Oct 12. Lancet Gastroenterol Hepatol. 2016. PMID: 28404095 Free PMC article. Review.
Historically, diabetes due to diseases of the exocrine pancreas was described as pancreatogenic or pancreatogenous diabetes mellitus, but recent literature refers to it as type 3c diabetes. It is important to note that type 3c diabetes is not a single entity; it occ …
Historically, diabetes due to diseases of the exocrine pancreas was described as pancreatogenic or pancreatogenous diabetes mellitus, but re …
Juvenile hemochromatosis.
Camaschella C, Roetto A, De Gobbi M. Camaschella C, et al. Semin Hematol. 2002 Oct;39(4):242-8. doi: 10.1053/shem.2002.35635. Semin Hematol. 2002. PMID: 12382199 Review.
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload earlier in life than HFE-related hemochromatosis. ...The disease is usually progressive and if untreated may become fatal beca …
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron ov …
Renal tubular dysgenesis.
Gubler MC. Gubler MC. Pediatr Nephrol. 2014 Jan;29(1):51-9. doi: 10.1007/s00467-013-2480-1. Epub 2013 May 1. Pediatr Nephrol. 2014. PMID: 23636579 Review.
Inherited RTD is genetically heterogeneous and linked to mutations in the genes encoding the major components of the renin-angiotensin system (RAS): angiotensinogen, renin, angiotensin-converting enzyme or angiotensin II receptor type 1. Mutations result in either t …
Inherited RTD is genetically heterogeneous and linked to mutations in the genes encoding the major components of the renin-angiotensin syste …
Hyperferritinemia in autoimmunity.
Zandman-Goddard G, Shoenfeld Y. Zandman-Goddard G, et al. Isr Med Assoc J. 2008 Jan;10(1):83-4. Isr Med Assoc J. 2008. PMID: 18300583 Free article. Review.
The immunological actions of ferritin include binding to T lymphocytes, suppression of the delayed-type hypersensitivity, suppression of antibody production by B lymphocytes, and decreased phagocytosis of granulocytes. Thyroid hormone, insulin and insulin growth factor- …
The immunological actions of ferritin include binding to T lymphocytes, suppression of the delayed-type hypersensitivity, suppression …
[Porphyria cutanea tara].
Merk HF. Merk HF. Hautarzt. 2016 Mar;67(3):207-10. doi: 10.1007/s00105-015-3744-4. Hautarzt. 2016. PMID: 26743054 Review. German.
Porphyria cutanea tara (PCT) has a prevelance of about 40 new diagnoses per 1 million people per year and is the most frequently occurring type of porphyria worldwide. ...Risk factors include alcohol, estrogen, iron overload, and hemochromatosis, hepatitis C …
Porphyria cutanea tara (PCT) has a prevelance of about 40 new diagnoses per 1 million people per year and is the most frequently occu …
Hepatobiliary pathology.
Lefkowitch JH. Lefkowitch JH. Curr Opin Gastroenterol. 2006 May;22(3):198-208. doi: 10.1097/01.mog.0000218955.55688.af. Curr Opin Gastroenterol. 2006. PMID: 16550033 Review.
RECENT FINDINGS: Two microscopic forms of pediatric nonalcoholic steatohepatitis have been described: type 1 in which hepatocyte ballooning and/or pericellular fibrosis accompany the steatosis; and type 2 which has portal tract inflammation and/or fibrosis as …
RECENT FINDINGS: Two microscopic forms of pediatric nonalcoholic steatohepatitis have been described: type 1 in which hepatocy …
Genetic hemochromatosis: Pathophysiology, diagnostic and therapeutic management.
Brissot P, Cavey T, Ropert M, Guggenbuhl P, Loréal O. Brissot P, et al. Presse Med. 2017 Dec;46(12 Pt 2):e288-e295. doi: 10.1016/j.lpm.2017.05.037. Epub 2017 Nov 20. Presse Med. 2017. PMID: 29158016 Review.
In contrast, iron excess in type 4A ferroportin disease is related to decreased cellular iron export. ...The mainstay of the treatment remains venesection therapy with the perspective of hepcidin supplementation for hepcidin deprivation-related HC. Prevention of HC is crit …
In contrast, iron excess in type 4A ferroportin disease is related to decreased cellular iron export. ...The mainstay of the treatmen …
Hereditary hemochromatosis.
Ajioka RS, Kushner JP. Ajioka RS, et al. Semin Hematol. 2002 Oct;39(4):235-41. doi: 10.1053/shem.2002.35634. Semin Hematol. 2002. PMID: 12382198 Review.
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by hyperabsorption of dietary iron. ...The prevalence of organ damage due to iron overload, however, remains a controversial issue. Published estimate …
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by hyperab …
Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: A case report and a review of the literature.
Zhang W, Lv T, Huang J, Ou X. Zhang W, et al. Medicine (Baltimore). 2017 Sep;96(38):e8064. doi: 10.1097/MD.0000000000008064. Medicine (Baltimore). 2017. PMID: 28930842 Free PMC article. Review.
Recently, non-HFE-related hemochromatosis has been reported in patients from the Asian countries. ...Functional analysis showed that IVS 3+10 del gtt in the SLC40A1 gene lead to a substantial reduction in the basal levels of SLC40A1 mRNA and increased membrane localization …
Recently, non-HFE-related hemochromatosis has been reported in patients from the Asian countries. ...Functional analysis showed that …
Current approach to hemochromatosis.
Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, Loréal O. Brissot P, et al. Blood Rev. 2008 Jul;22(4):195-210. doi: 10.1016/j.blre.2008.03.001. Epub 2008 Apr 21. Blood Rev. 2008. PMID: 18430498 Review.
Five major categories are now established: HFE-related or type1 hemochromatosis, frequently found in Caucasians, and four rarer diseases which are type 2 (A and B) hemochromatosis (juvenile hemochromatosis), type 3 hemochromatosis (transf …
Five major categories are now established: HFE-related or type1 hemochromatosis, frequently found in Caucasians, and four rarer disea …
91 results