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Year Number of Results
1948 1
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1980 6
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1982 2
1983 5
1984 4
1985 4
1986 3
1987 1
1988 3
1989 1
1990 1
1991 4
1992 3
1993 6
1994 3
1995 4
1996 3
1997 6
1998 5
1999 7
2000 13
2001 12
2002 6
2003 10
2004 14
2005 9
2006 10
2007 10
2008 14
2009 12
2010 16
2011 14
2012 23
2013 19
2014 28
2015 23
2016 28
2017 27
2018 24
2019 27
2020 29
2021 39
2022 42
2023 39
2024 10

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525 results

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Page 1
Wolfram Syndrome: Diagnosis, Management, and Treatment.
Urano F. Urano F. Curr Diab Rep. 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6. Curr Diab Rep. 2016. PMID: 26742931 Free PMC article. Review.
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing loss, and neurodegeneration. ...The prognosis of this syndrome is currently poor, and many patients die prematurely …
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve …
Wolfram Syndrome 1: From Genetics to Therapy.
Rigoli L, Caruso V, Salzano G, Lombardo F. Rigoli L, et al. Int J Environ Res Public Health. 2022 Mar 9;19(6):3225. doi: 10.3390/ijerph19063225. Int J Environ Res Public Health. 2022. PMID: 35328914 Free PMC article. Review.
Wolfram syndrome 1 (WS1) is a rare neurodegenerative disease transmitted in an autosomal recessive mode. ...However, abnormal phenotypes of WS with or without DM, inherited in an autosomal dominant mode and associated with one or more WFS1 mutations, have bee …
Wolfram syndrome 1 (WS1) is a rare neurodegenerative disease transmitted in an autosomal recessive mode. ...However, ab …
Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C, Brink JBT, Bergen AA, Boon CJF, van Genderen MM. de Muijnck C, et al. Surv Ophthalmol. 2023 Jul-Aug;68(4):641-654. doi: 10.1016/j.survophthal.2023.01.012. Epub 2023 Feb 9. Surv Ophthalmol. 2023. PMID: 36764396 Free article. Review.
Wolfram-like syndrome (WFLS) is a recently described autosomal dominant disorder with phenotypic similarities to autosomal recessive Wolfram syndrome (WS), including optic atrophy, hearing impairment, and diabetes mellitus. ...
Wolfram-like syndrome (WFLS) is a recently described autosomal dominant disorder with phenotypic similarities to autosomal rec …
Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives.
Pallotta MT, Tascini G, Crispoldi R, Orabona C, Mondanelli G, Grohmann U, Esposito S. Pallotta MT, et al. J Transl Med. 2019 Jul 23;17(1):238. doi: 10.1186/s12967-019-1993-1. J Transl Med. 2019. PMID: 31337416 Free PMC article. Review.
BACKGROUND: Wolfram syndrome (WS), a rare genetic disorder, is considered the best prototype of endoplasmic reticulum (ER) diseases. ...Being a monogenic pathology, WS represents a perfect model to study the mechanisms of ER stress and how this condition lead …
BACKGROUND: Wolfram syndrome (WS), a rare genetic disorder, is considered the best prototype of endoplasmic reticulum (ER) …
Wolfram Syndrome: Only a Neurodegenerative Disease or Also a Maculopathy?
Tombolini B, Battista M, Borrelli E, Frontino G, Bandello F, Barboni P, Cascavilla ML. Tombolini B, et al. J Neuroophthalmol. 2023 Aug 14. doi: 10.1097/WNO.0000000000001981. Online ahead of print. J Neuroophthalmol. 2023. PMID: 37581949 No abstract available.
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.
Rigoli L, Bramanti P, Di Bella C, De Luca F. Rigoli L, et al. Pediatr Res. 2018 May;83(5):921-929. doi: 10.1038/pr.2018.17. Epub 2018 Feb 28. Pediatr Res. 2018. PMID: 29774890 Review.
Wolfram syndrome 1 (WS1) is a rare autosomal recessive neurodegenerative disease characterized by diabetes insipidus, diabetes mellitus, optic atrophy, deafness, and other abnormalities. ...Other WFS1-related disorders such as DFNA6/14/38 nonsyndromic low-fre …
Wolfram syndrome 1 (WS1) is a rare autosomal recessive neurodegenerative disease characterized by diabetes insipidus, d …
Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer's disease.
Li L, Venkataraman L, Chen S, Fu H. Li L, et al. Neurosci Biobehav Rev. 2020 Nov;118:775-783. doi: 10.1016/j.neubiorev.2020.09.011. Epub 2020 Sep 17. Neurosci Biobehav Rev. 2020. PMID: 32949681 Free PMC article. Review.
Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer's Disease. NEUROSCI BIOBEHAV REVXXX-XXX,2020....Most WS patients belong to Wolfram Syndrome type 1 (WS1) caused by mutations in the Wolfr …
Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer's Disease. NEU …
Comprehensive overview of disease models for Wolfram syndrome: toward effective treatments.
Morikawa S, Tanabe K, Kaneko N, Hishimura N, Nakamura A. Morikawa S, et al. Mamm Genome. 2024 Mar;35(1):1-12. doi: 10.1007/s00335-023-10028-x. Epub 2024 Feb 13. Mamm Genome. 2024. PMID: 38351344 Review.
Wolfram syndrome (OMIM 222300) is a rare autosomal recessive disease with a devastating array of symptoms, including diabetes mellitus, optic nerve atrophy, diabetes insipidus, hearing loss, and neurological dysfunction. ...To bridge these knowledge gaps, …
Wolfram syndrome (OMIM 222300) is a rare autosomal recessive disease with a devastating array of symptoms, including di …
Wolfram syndrome: MAMs' connection?
Delprat B, Maurice T, Delettre C. Delprat B, et al. Cell Death Dis. 2018 Mar 6;9(3):364. doi: 10.1038/s41419-018-0406-3. Cell Death Dis. 2018. PMID: 29511163 Free PMC article. Review.
Wolfram syndrome (WS) is a rare neurodegenerative disease, the main pathological hallmarks of which associate with diabetes, optic atrophy, and deafness. ...ER contacts mitochondria to ensure effective Ca(2+) transfer, lipids transfer, and apoptosis within st …
Wolfram syndrome (WS) is a rare neurodegenerative disease, the main pathological hallmarks of which associate with diab …
Dysregulated Ca(2+) Homeostasis as a Central Theme in Neurodegeneration: Lessons from Alzheimer's Disease and Wolfram Syndrome.
Callens M, Loncke J, Bultynck G. Callens M, et al. Cells. 2022 Jun 18;11(12):1963. doi: 10.3390/cells11121963. Cells. 2022. PMID: 35741091 Free PMC article. Review.
In this review, we focus on the emerging role of Ca(2+) signaling at the ER-mitochondrial interface in two different neurodegenerative diseases, namely Alzheimer's disease and Wolfram syndrome. Both of these diseases share some common hallmarks …
In this review, we focus on the emerging role of Ca(2+) signaling at the ER-mitochondrial interface in two different neurodegenerative di …
525 results