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

Year Number of Results
1984 2
1986 1
1987 3
1988 3
1994 3
1995 1
1996 4
1997 9
1998 10
1999 7
2000 9
2001 10
2002 2
2003 6
2004 2
2005 5
2006 3
2007 3
2008 5
2009 9
2010 8
2011 10
2012 14
2013 17
2014 13
2015 20
2016 24
2017 11
2018 11
2019 21
2020 17
2021 18
2022 22
2023 16
2024 12
2025 4
2026 1

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297 results

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Page 1
Alzheimer's disease: a comprehensive review of epidemiology, risk factors, symptoms diagnosis, management, caregiving, advanced treatments and associated challenges.
Safiri S, Ghaffari Jolfayi A, Fazlollahi A, Morsali S, Sarkesh A, Daei Sorkhabi A, Golabi B, Aletaha R, Motlagh Asghari K, Hamidi S, Mousavi SE, Jamalkhani S, Karamzad N, Shamekh A, Mohammadinasab R, Sullman MJM, Şahin F, Kolahi AA. Safiri S, et al. Front Med (Lausanne). 2024 Dec 16;11:1474043. doi: 10.3389/fmed.2024.1474043. eCollection 2024. Front Med (Lausanne). 2024. PMID: 39736972 Free PMC article. Review.
BACKGROUND: Alzheimer's disease (AD) is a chronic, progressive neurodegenerative disorder characterized by cognitive decline, memory loss, and impaired reasoning. ...The National Institute on Aging and the Alzheimer's Association have updated diagnostic criteria to …
BACKGROUND: Alzheimer's disease (AD) is a chronic, progressive neurodegenerative disorder characterized by cognitive decline, memory …
Schwann cells contribute to keloid formation.
Direder M, Weiss T, Copic D, Vorstandlechner V, Laggner M, Pfisterer K, Mildner CS, Klas K, Bormann D, Haslik W, Radtke C, Farlik M, Shaw L, Golabi B, Tschachler E, Hoetzenecker K, Ankersmit HJ, Mildner M. Direder M, et al. Matrix Biol. 2022 Apr;108:55-76. doi: 10.1016/j.matbio.2022.03.001. Epub 2022 Mar 10. Matrix Biol. 2022. PMID: 35278628 Free article.
Simpson-Golabi-Behmel syndrome types I and II.
Tenorio J, Arias P, Martínez-Glez V, Santos F, García-Miñaur S, Nevado J, Lapunzina P. Tenorio J, et al. Orphanet J Rare Dis. 2014 Sep 20;9:138. doi: 10.1186/s13023-014-0138-0. Orphanet J Rare Dis. 2014. PMID: 25238977 Free PMC article. Review.
Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pre/postnatal overgrowth, distinctive craniofacial features, macrocephaly, and organomegaly. ...
Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pr …
Prevalence of metabolic dysfunction-associated steatotic liver disease in the Middle East and North Africa.
Younossi ZM, Golabi P, Paik J, Owrangi S, Yilmaz Y, El-Kassas M, Alswat K, Alqahtani SA. Younossi ZM, et al. Liver Int. 2024 Apr;44(4):1061-1070. doi: 10.1111/liv.15852. Epub 2024 Feb 2. Liver Int. 2024. PMID: 38305642
METHODS: We searched PubMed and Embase for English-language articles published between 1990 and 2023 according to PRISMA. Each country's NAFLD/MASLD prevalence in the general population and in T2D patients was predicted by using a multivariable meta regression model. ...
METHODS: We searched PubMed and Embase for English-language articles published between 1990 and 2023 according to PRISMA. Each country's …
Simpson-Golabi-Behmel syndrome in one of the Dichorionic-diamniotic twin: a case report and literature review.
Guo Y, Zhang H, Fan L, Chen J, Zhang X, Yang H, Sun Y. Guo Y, et al. BMC Pregnancy Childbirth. 2022 Jan 17;22(1):42. doi: 10.1186/s12884-021-04309-z. BMC Pregnancy Childbirth. 2022. PMID: 35038998 Free PMC article. Review.
BACKGROUND: Simpson-Golabi-Behmel syndrome (SGBS) is a rare X-linked overgrowth syndrome. The main clinical manifestations are overgrowth and multiple malformations. ...Clinicians need to be more aware of typical SGBS's clinical findings and choose genetic testing m …
BACKGROUND: Simpson-Golabi-Behmel syndrome (SGBS) is a rare X-linked overgrowth syndrome. The main clinical manifestations are overgr …
Prenatal diagnosis of Simpson-Golabi-Behmel syndrome.
Magini P, Palombo F, Boito S, Lanzoni G, Mongelli P, Rizzuti T, Baccarin M, Pippucci T, Seri M, Lalatta F. Magini P, et al. Am J Med Genet A. 2016 Dec;170(12):3258-3264. doi: 10.1002/ajmg.a.37873. Epub 2016 Sep 9. Am J Med Genet A. 2016. PMID: 27612164
Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth syndrome and it is usually diagnosed postnatally, on the basis of phenotype. ...
Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth syndrome and it is usually diagnosed postnatally, on the basis of phenotype. . …
The Terry Fox Research Institute Marathon of Hope Cancer Centres Network: A pan-Canadian precision oncology initiative.
Terry Fox Research Institute Marathon of Hope Cancer Centers Network. Electronic address: mmarra@bcgsc.ca; Terry Fox Research Institute Marathon of Hope Cancer Centers Network. Terry Fox Research Institute Marathon of Hope Cancer Centers Network. Electronic address: mmarra@bcgsc.ca, et al. Cancer Cell. 2025 Apr 14;43(4):587-592. doi: 10.1016/j.ccell.2025.03.014. Epub 2025 Apr 3. Cancer Cell. 2025. PMID: 40185094 Review.
The Marathon of Hope Cancer Centres Network (MOHCCN), led by the Terry Fox Research Institute and the Terry Fox Foundation, unites researchers, clinicians, patients, funders, and other partners across Canada to accelerate precision oncology, promote collaboration and data sharing …
The Marathon of Hope Cancer Centres Network (MOHCCN), led by the Terry Fox Research Institute and the Terry Fox Foundation, unites researche …
297 results