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

Year Number of Results
1958 1
1967 2
1968 3
1969 3
1970 3
1971 3
1972 1
1975 1
1976 2
1977 1
1978 3
1979 2
1980 1
1981 1
1984 1
1986 2
1988 2
1989 2
1990 1
2004 1
2006 1
2008 1
2009 1
2011 1
2014 1
2020 3
2021 2
2023 1
2024 0

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45 results

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Page 1
Episodic Ataxias: Primary and Secondary Etiologies, Treatment, and Classification Approaches.
Hassan A. Hassan A. Tremor Other Hyperkinet Mov (N Y). 2023 Mar 28;13:9. doi: 10.5334/tohm.747. eCollection 2023. Tremor Other Hyperkinet Mov (N Y). 2023. PMID: 37008993 Free PMC article. Review.
METHODS: A systematic literature review was performed in October 2022 for 'episodic ataxia' and 'paroxysmal ataxia', restricted to publications in the last 10 years to focus on recent clinical advances. Clinical, genetic, and treatment characteristics were summarize …
METHODS: A systematic literature review was performed in October 2022 for 'episodic ataxia' and 'paroxysmal ataxia', restricted to publicati …
Pellagra a review exploring causes and mechanisms, including isoniazid-induced pellagra.
Prabhu D, Dawe RS, Mponda K. Prabhu D, et al. Photodermatol Photoimmunol Photomed. 2021 Mar;37(2):99-104. doi: 10.1111/phpp.12659. Epub 2021 Feb 2. Photodermatol Photoimmunol Photomed. 2021. PMID: 33471377 Review.
Pellagra is a clinical syndrome caused by a deficiency of niacin (nicotinic acid) and/or its precursor tryptophan. ...
Pellagra is a clinical syndrome caused by a deficiency of niacin (nicotinic acid) and/or its precursor tryptophan. ...
Biochemical phenotyping of multiple myeloma patients at diagnosis reveals a disorder of mitochondrial complexes I and II and a Hartnup-like disturbance as underlying conditions, also influencing different stages of the disease.
da Silva IDCG, de Castro Levatti EV, Pedroso AP, Marchioni DML, Carioca AAF, Colleoni GWB. da Silva IDCG, et al. Sci Rep. 2020 Dec 14;10(1):21836. doi: 10.1038/s41598-020-75862-4. Sci Rep. 2020. PMID: 33318510 Free PMC article. Clinical Trial.
In conclusion, our study showed that MM patients at diagnosis showed metabolic disorders resembling both mitochondrial complexes I and II and Hartnup-like disturbances as underlying conditions, also influencing different stages of the disease....
In conclusion, our study showed that MM patients at diagnosis showed metabolic disorders resembling both mitochondrial complexes I and II an …
Influenza vaccination strategies for 2020-21 in the context of COVID-19.
Wang X, Kulkarni D, Dozier M, Hartnup K, Paget J, Campbell H, Nair H; Usher Network for COVID-19 Evidence Reviews (UNCOVER) group. Wang X, et al. J Glob Health. 2020 Dec;10(2):021102. doi: 10.7189/jogh.10.021102. J Glob Health. 2020. PMID: 33312512 Free PMC article.
COVID-19 and Hartnup disease: an affair of intestinal amino acid malabsorption.
Nisoli E, Cinti S, Valerio A. Nisoli E, et al. Eat Weight Disord. 2021 Jun;26(5):1647-1651. doi: 10.1007/s40519-020-00963-y. Epub 2020 Jul 20. Eat Weight Disord. 2021. PMID: 32691334 Free PMC article.
Since the outbreak of COVID-19, clinicians have tried every effort to fight the disease, and multiple drugs have been proposed. However, no proven effective therapies currently exist, and different clinical phenotypes complicate the situation. ...Understanding the m …
Since the outbreak of COVID-19, clinicians have tried every effort to fight the disease, and multiple drugs have been proposed. Howev …
Severe persistent unremitting dermatitis, chronic diarrhea and hypoalbuminemia in a child; Hartnup disease in setting of celiac disease.
Ciecierega T, Dweikat I, Awar M, Shahrour M, Libdeh BA, Sultan M. Ciecierega T, et al. BMC Pediatr. 2014 Dec 20;14:311. doi: 10.1186/s12887-014-0311-6. BMC Pediatr. 2014. PMID: 25526748 Free PMC article.
Hartnup disease is an autosomal recessive disorder caused by increased urinary excretion of neutral amino acids. Co-occurrence of Hartnup disease and CD is extremely rare with only a single case reported. ...
Hartnup disease is an autosomal recessive disorder caused by increased urinary excretion of neutral amino acids. Co-occurrence
Amino acid absorption and homeostasis in mice lacking the intestinal peptide transporter PEPT1.
Nässl AM, Rubio-Aliaga I, Fenselau H, Marth MK, Kottra G, Daniel H. Nässl AM, et al. Am J Physiol Gastrointest Liver Physiol. 2011 Jul;301(1):G128-37. doi: 10.1152/ajpgi.00017.2011. Epub 2011 Feb 24. Am J Physiol Gastrointest Liver Physiol. 2011. PMID: 21350187 Free article.
Whereas the transporter appears to be essential to compensate for the reduced amino acid delivery in patients with mutations in amino acid transporter genes, such as in cystinuria or Hartnup disease, its physiological role in overall amino acid absorption is still n …
Whereas the transporter appears to be essential to compensate for the reduced amino acid delivery in patients with mutations in amino acid t …
Severe exfoliative erythema of malnutrition in a child with coexisting coeliac and Hartnup's disease.
Sander CS, Hertecant J, Abdulrazzaq YM, Berger TG. Sander CS, et al. Clin Exp Dermatol. 2009 Mar;34(2):178-82. doi: 10.1111/j.1365-2230.2008.02773.x. Epub 2008 Nov 6. Clin Exp Dermatol. 2009. PMID: 19018792
We report a 3-year-old Iraqi girl with malnutrition due to coexisting coeliac and Hartnup's disease. On admission to hospital, she presented with kwashiorkor, anaemia, hepatitis and hypoalbuminia. ...
We report a 3-year-old Iraqi girl with malnutrition due to coexisting coeliac and Hartnup's disease. On admission to hospital, …
Spontaneous scalp arteriovenous fistula in a child with hartnup disease.
Kim DM, Benndorf G, Von Moers A, Campi A, Lehmann TN. Kim DM, et al. J Endovasc Ther. 2004 Jun;11(3):348-50. doi: 10.1583/03-1123.1. J Endovasc Ther. 2004. PMID: 15174904
PURPOSE: To report the endovascular treatment of a spontaneous scalp arteriovenous fistula (AVF) in a child with Hartnup disease. CASE REPORT: A 6-year-old girl with Hartnup disease presented with recurrent attacks of intense, migraine-like, right-side …
PURPOSE: To report the endovascular treatment of a spontaneous scalp arteriovenous fistula (AVF) in a child with Hartnup disease
45 results