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
1948 1
1949 1
1950 1
1954 3
1955 1
1956 1
1957 3
1958 1
1959 1
1961 2
1963 2
1965 1
1966 1
1967 1
1970 1
1972 3
1973 2
1974 3
1975 2
1976 1
1977 2
1978 1
1979 1
1982 1
1983 2
1984 8
1985 3
1986 2
1987 3
1988 3
1989 6
1990 9
1991 3
1992 2
1993 6
1994 5
1995 8
1996 5
1997 5
1998 5
1999 4
2000 10
2001 8
2002 7
2003 6
2004 8
2005 7
2006 13
2007 28
2008 25
2009 30
2010 17
2011 30
2012 36
2013 26
2014 29
2015 42
2016 31
2017 30
2018 29
2019 26
2020 34
2021 43
2022 52
2023 49
2024 23

Text availability

Article attribute

Article type

Publication date

Search Results

668 results

Results by year

Filters applied: . Clear all
Page 1
Showing results for alstrom
Your search for altrom retrieved no results
Alstrom Syndrome.
Paisey RB, Steeds R, Barrett T, Williams D, Geberhiwot T, Gunay-Aygun M. Paisey RB, et al. 2003 Feb 7 [updated 2019 Jun 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Feb 7 [updated 2019 Jun 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301444 Free Books & Documents. Review.
The molecular diagnosis of Alstrom syndrome is established in individuals of all ages by identification of biallelic pathogenic variants in ALMS1 on molecular genetic testing. MANAGEMENT: Treatment of manifestations: No therapy exists to prevent the progressive organ invol …
The molecular diagnosis of Alstrom syndrome is established in individuals of all ages by identification of biallelic pathogenic varia …
Ciliopathy: Alstrom Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:179-180. doi: 10.1007/978-3-319-95046-4_35. Adv Exp Med Biol. 2018. PMID: 30578508 Review.
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 diabetes, insulin resistance with hyperinsulinemia, dilated cardiomyopathy, and progressive hepatic and renal failure. ...
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 d …
Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alstrom syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period.
Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J. Haqq AM, et al. Lancet Diabetes Endocrinol. 2022 Dec;10(12):859-868. doi: 10.1016/S2213-8587(22)00277-7. Epub 2022 Nov 7. Lancet Diabetes Endocrinol. 2022. PMID: 36356613 Free PMC article. Clinical Trial.
BACKGROUND: Impaired cilial signalling in the melanocortin-4 receptor (MC4R) pathway might contribute to obesity in patients with Bardet-Biedl syndrome and Alstrom syndrome, rare genetic diseases associated with hyperphagia and early-onset severe obesity. ...Patients aged …
BACKGROUND: Impaired cilial signalling in the melanocortin-4 receptor (MC4R) pathway might contribute to obesity in patients with Bardet-Bie …
A review of Alstrom syndrome: a rare monogenic ciliopathy.
Choudhury AR, Munonye I, Sanu KP, Islam N, Gadaga C. Choudhury AR, et al. Intractable Rare Dis Res. 2021 Nov;10(4):257-262. doi: 10.5582/irdr.2021.01113. Intractable Rare Dis Res. 2021. PMID: 34877237 Free PMC article. Review.
Alstrom syndrome is a rare monogenic ciliopathy caused by a mutation to the Alstrom syndrome 1 (ALMS1) gene. Alstrom syndrome has an autosomal recessive nature of inheritance. ...
Alstrom syndrome is a rare monogenic ciliopathy caused by a mutation to the Alstrom syndrome 1 (ALMS1) gene. Alstrom sy …
Alstrom syndrome: current perspectives.
Álvarez-Satta M, Castro-Sánchez S, Valverde D. Álvarez-Satta M, et al. Appl Clin Genet. 2015 Jul 21;8:171-9. doi: 10.2147/TACG.S56612. eCollection 2015. Appl Clin Genet. 2015. PMID: 26229500 Free PMC article. Review.
Alstrom syndrome (ALMS) is a rare genetic disorder that has been included in the ciliopathies group, in the last few years. ...
Alstrom syndrome (ALMS) is a rare genetic disorder that has been included in the ciliopathies group, in the last few years. ...
Alstrom syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity.
Dassie F, Favaretto F, Bettini S, Parolin M, Valenti M, Reschke F, Danne T, Vettor R, Milan G, Maffei P. Dassie F, et al. Endocrine. 2021 Mar;71(3):618-625. doi: 10.1007/s12020-021-02643-y. Epub 2021 Feb 10. Endocrine. 2021. PMID: 33566311 Review.
BACKGROUND: Alstrom syndrome (ALMS) is a monogenic ultra-rare disorder with a prevalence of one per million inhabitants caused by pathogenic variants of ALMS1 gene. ...
BACKGROUND: Alstrom syndrome (ALMS) is a monogenic ultra-rare disorder with a prevalence of one per million inhabitants caused by pat …
Alstrom syndrome.
Marshall JD, Beck S, Maffei P, Naggert JK. Marshall JD, et al. Eur J Hum Genet. 2007 Dec;15(12):1193-202. doi: 10.1038/sj.ejhg.5201933. Epub 2007 Oct 17. Eur J Hum Genet. 2007. PMID: 17940554
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently unknown molecular function. ...Most patients demonstrate normal intelligence, although some reports indicate delayed psychomotor and intellec …
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently u …
Alstrom syndrome: insights into the pathogenesis of metabolic disorders.
Girard D, Petrovsky N. Girard D, et al. Nat Rev Endocrinol. 2011 Feb;7(2):77-88. doi: 10.1038/nrendo.2010.210. Epub 2010 Dec 7. Nat Rev Endocrinol. 2011. PMID: 21135875 Review.
Genetic causes of obesity include the ciliopathies Alstrom syndrome and Bardet-Biedl syndrome. In these disorders, mutations cause dysfunction of the primary cilium, an organelle involved in intracellular and intercellular sensing and signaling. Alstrom syndrome is …
Genetic causes of obesity include the ciliopathies Alstrom syndrome and Bardet-Biedl syndrome. In these disorders, mutations cause dy …
Setmelanotide: First Approval.
Markham A. Markham A. Drugs. 2021 Feb;81(3):397-403. doi: 10.1007/s40265-021-01470-9. Drugs. 2021. PMID: 33638809 Review.
Setmelanotide is also being developed in other rare genetic disorders associated with obesity including Bardet-Biedl Syndrome, Alstrom Syndrome, POMC and other MC4R pathway heterozygous deficiency obesities, and POMC epigenetic disorders. ...
Setmelanotide is also being developed in other rare genetic disorders associated with obesity including Bardet-Biedl Syndrome, Alstrom …
ALMS1 and Alstrom syndrome: a recessive form of metabolic, neurosensory and cardiac deficits.
Hearn T. Hearn T. J Mol Med (Berl). 2019 Jan;97(1):1-17. doi: 10.1007/s00109-018-1714-x. Epub 2018 Nov 12. J Mol Med (Berl). 2019. PMID: 30421101 Free PMC article. Review.
Alstrom syndrome (AS) is characterised by metabolic deficits, retinal dystrophy, sensorineural hearing loss, dilated cardiomyopathy and multi-organ fibrosis. ...
Alstrom syndrome (AS) is characterised by metabolic deficits, retinal dystrophy, sensorineural hearing loss, dilated cardiomyopathy a …
668 results