Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1983 1
1987 2
1988 1
1991 2
1992 2
1993 2
1994 1
1995 1
1996 1
1997 1
2000 2
2002 2
2004 2
2005 1
2006 1
2011 1
2012 2
2017 3
2018 2
2020 3
2022 1
2023 1

Text availability

Article attribute

Article type

Publication date

Search Results

33 results

Results by year

Filters applied: . Clear all
Page 1
Human Ascariasis: An Updated Review.
Leung AKC, Leung AAM, Wong AHC, Hon KL. Leung AKC, et al. Recent Pat Inflamm Allergy Drug Discov. 2020;14(2):133-145. doi: 10.2174/1872213X14666200705235757. Recent Pat Inflamm Allergy Drug Discov. 2020. PMID: 32628606 Review.
For those with symptoms, anorexia, nausea, bloating, abdominal discomfort, recurrent abdominal pain, abdominal distension, and intermittent diarrhea are not uncommon. Other clinical manifestations vary widely, depending on the underlying complications. Complications includ …
For those with symptoms, anorexia, nausea, bloating, abdominal discomfort, recurrent abdominal pain, abdominal distension, and intermitte …
Gilbert syndrome.
Fretzayas A, Moustaki M, Liapi O, Karpathios T. Fretzayas A, et al. Eur J Pediatr. 2012 Jan;171(1):11-5. doi: 10.1007/s00431-011-1641-0. Epub 2011 Dec 9. Eur J Pediatr. 2012. PMID: 22160004 Review.
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. ...In its typical form, hyperbilirubinemia is first noti …
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unc …
Intermittent phototherapy versus continuous phototherapy for neonatal jaundice.
Gottimukkala SB, Lobo L, Gautham KS, Bolisetty S, Fiander M, Schindler T. Gottimukkala SB, et al. Cochrane Database Syst Rev. 2023 Mar 2;3(3):CD008168. doi: 10.1002/14651858.CD008168.pub2. Cochrane Database Syst Rev. 2023. PMID: 36867730 Review.
BACKGROUND: Phototherapy is a widely accepted, effective first-line therapy for neonatal jaundice. It is traditionally used continuously but intermittent phototherapy has been proposed as an equally effective alternative with practical advantages of improved materna …
BACKGROUND: Phototherapy is a widely accepted, effective first-line therapy for neonatal jaundice. It is traditionally used continuou …
New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications.
Sticova E, Jirsa M, Pawłowska J. Sticova E, et al. Can J Gastroenterol Hepatol. 2018 Jul 26;2018:2313675. doi: 10.1155/2018/2313675. eCollection 2018. Can J Gastroenterol Hepatol. 2018. PMID: 30148122 Free PMC article. Review.
Hereditary cholestasis is a heterogeneous group of rare autosomal recessive liver disorders, which are characterised by intrahepatic cholestasis, pruritus, and jaundice and caused by defects in genes related to the secretion and transport of bile salts and lipids. Phenotyp …
Hereditary cholestasis is a heterogeneous group of rare autosomal recessive liver disorders, which are characterised by intrahepatic cholest …
Ticlopidine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in platelet-dependent disease states.
Saltiel E, Ward A. Saltiel E, et al. Drugs. 1987 Aug;34(2):222-62. doi: 10.2165/00003495-198734020-00003. Drugs. 1987. PMID: 3304967 Review.
Therapeutic trials in patients with chronic arterial occlusion due to thrombangitis obliterans or arteriosclerosis obliterans, post-myocardial infarction, cerebrovascular thromboembolic disease, subarachnoid haemorrhage, vascular shunts or fistulas for haemodialysis, and sickle c …
Therapeutic trials in patients with chronic arterial occlusion due to thrombangitis obliterans or arteriosclerosis obliterans, post-myocardi …
Hereditary elliptocytosis: spectrin and protein 4.1R.
Gallagher PG. Gallagher PG. Semin Hematol. 2004 Apr;41(2):142-64. doi: 10.1053/j.seminhematol.2004.01.003. Semin Hematol. 2004. PMID: 15071791 Review.
The majority of HE patients are asymptomatic, but some may experience hemolytic anemia, splenomegaly, and intermittent jaundice....
The majority of HE patients are asymptomatic, but some may experience hemolytic anemia, splenomegaly, and intermittent jaundice …
Recent advances in pancreaticobiliary maljunction.
Matsumoto Y, Fujii H, Itakura J, Matsuda M, Nobukawa B, Suda K. Matsumoto Y, et al. J Hepatobiliary Pancreat Surg. 2002;9(1):45-54. doi: 10.1007/s005340200004. J Hepatobiliary Pancreat Surg. 2002. PMID: 12021897 Review.
However, in PBM patients with a short common duct (less than 1 cm in length), detection of the extramural location is difficult. The clinical features of PBM are intermittent abdominal pain, with or without elevation of pancreatic enzyme levels; and obstructive jaundice …
However, in PBM patients with a short common duct (less than 1 cm in length), detection of the extramural location is difficult. The clinica …
Hepatitis C: the clinical spectrum of disease.
Hoofnagle JH. Hoofnagle JH. Hepatology. 1997 Sep;26(3 Suppl 1):15S-20S. doi: 10.1002/hep.510260703. Hepatology. 1997. PMID: 9305658 Review.
Probably fewer than 20% of patients have symptoms and they are usually intermittent, vague, and nonspecific, largely being malaise and easy fatiguability. ...Once cirrhosis develops, symptoms are more common and the signs of end-stage liver disease can appear with jaund …
Probably fewer than 20% of patients have symptoms and they are usually intermittent, vague, and nonspecific, largely being malaise an …
Research Advances in Clinical and Imaging Characteristics of Intraductal Papillary Mucinous Neoplasm of the Bile Duct.
He MN, Zhang J, Zhang Q, Lv K, Jiang YX. He MN, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2017 Jun 20;39(3):451-455. doi: 10.3881/j.issn.1000-503X.2017.03.026. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2017. PMID: 28695820 Review.
This review summarizes some of the typical cases reported since 2000 and find that clinical manifestations of IPMN-B include epigastric discomfort,biliary colic,jaundice,intermittent fever,sometimes without any symptoms; imaging triads for IPMN-B are mucobilia,dilat …
This review summarizes some of the typical cases reported since 2000 and find that clinical manifestations of IPMN-B include epigastric disc …
Neonatal cholestatic conditions requiring surgical reconstruction.
Ryckman FC, Noseworthy J. Ryckman FC, et al. Semin Liver Dis. 1987 May;7(2):134-54. doi: 10.1055/s-2008-1040572. Semin Liver Dis. 1987. PMID: 3303345 Review.
Obstructive jaundice in infancy and childhood can arise from a variety of causes. ...Episodes of intermittent jaundice or persistent conjugated hyperbilirubinemia should be investigated at any age to exclude obstructive lesions of the extrahepatic biliary tra …
Obstructive jaundice in infancy and childhood can arise from a variety of causes. ...Episodes of intermittent jaundice …
33 results