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Year Number of Results
1949 1
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1962 1
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1967 1
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1986 1
1991 1
1992 2
1994 2
1995 2
1996 2
1997 2
1998 2
1999 3
2000 2
2001 4
2002 5
2003 4
2004 5
2005 6
2006 6
2007 6
2008 8
2009 7
2010 10
2011 13
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2013 20
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2025 1

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282 results

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Page 1
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study.
Canton APM, Tinano FR, Guasti L, Montenegro LR, Ryan F, Shears D, de Melo ME, Gomes LG, Piana MP, Brauner R, Espino-Aguilar R, Escribano-Muñoz A, Paganoni A, Read JE, Korbonits M, Seraphim CE, Costa SS, Krepischi AC, Jorge AAL, David A, Kaisinger LR, Ong KK, Perry JRB, Abreu AP, Kaiser UB, Argente J, Mendonca BB, Brito VN, Howard SR, Latronico AC. Canton APM, et al. Among authors: montenegro lr. Lancet Diabetes Endocrinol. 2023 Aug;11(8):545-554. doi: 10.1016/S2213-8587(23)00131-6. Epub 2023 Jun 26. Lancet Diabetes Endocrinol. 2023. PMID: 37385287 Free PMC article.
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. Granadillo JL, et al. Among authors: montenegro l. J Med Genet. 2020 Oct;57(10):717-724. doi: 10.1136/jmedgenet-2019-106470. Epub 2020 Mar 9. J Med Genet. 2020. PMID: 32152250
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases.
Corben LA, Collins V, Milne S, Farmer J, Musheno A, Lynch D, Subramony S, Pandolfo M, Schulz JB, Lin K, Delatycki MB; Clinical Management Guidelines Writing Group. Corben LA, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):415. doi: 10.1186/s13023-022-02568-3. Orphanet J Rare Dis. 2022. PMID: 36371255 Free PMC article.
The genetic etiology is a relevant cause of central precocious puberty.
Canton APM, Seraphim CE, Montenegro LR, Krepischi ACV, Mendonca BB, Latronico AC, Brito VN. Canton APM, et al. Among authors: montenegro lr. Eur J Endocrinol. 2024 Jun 5;190(6):479-488. doi: 10.1093/ejendo/lvae063. Eur J Endocrinol. 2024. PMID: 38857188
Intravenous magnesium: Are we crossing the limits?
Subramanyam R, Romer AJ, Montenegro L. Subramanyam R, et al. Among authors: montenegro l. Paediatr Anaesth. 2022 Apr;32(4):494-496. doi: 10.1111/pan.14405. Paediatr Anaesth. 2022. PMID: 35343036 No abstract available.
Sagittal reduction genioplasty: Technical note.
Lagos OAV, Montenegro L, Colucci G, Amarista FJ. Lagos OAV, et al. Among authors: montenegro l. J Stomatol Oral Maxillofac Surg. 2022 Oct;123(5):576-580. doi: 10.1016/j.jormas.2022.02.015. Epub 2022 Feb 28. J Stomatol Oral Maxillofac Surg. 2022. PMID: 35240341
Fundamentals and practice of care in Gerontological Nursing.
Polaro SHI, Montenegro LC. Polaro SHI, et al. Among authors: montenegro lc. Rev Bras Enferm. 2017 Jul-Aug;70(4):671-672. doi: 10.1590/0034-7167.2017700401. Rev Bras Enferm. 2017. PMID: 28793093 Free article. English, Portuguese, Spanish. No abstract available.
Clinical and Genetic Characterization of Familial Central Precocious Puberty.
Tinano FR, Canton APM, Montenegro LR, de Castro Leal A, Faria AG, Seraphim CE, Brauner R, Jorge AA, Mendonca BB, Argente J, Brito VN, Latronico AC. Tinano FR, et al. Among authors: montenegro lr. J Clin Endocrinol Metab. 2023 Jun 16;108(7):1758-1767. doi: 10.1210/clinem/dgac763. J Clin Endocrinol Metab. 2023. PMID: 36611250
282 results