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

Year Number of Results
1997 1
1999 2
2000 3
2001 2
2002 2
2003 4
2004 2
2005 2
2006 3
2007 5
2008 3
2009 5
2010 6
2011 5
2012 3
2013 9
2014 6
2015 4
2016 6
2017 6
2018 12
2019 6
2020 10
2021 6
2022 9
2023 9

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111 results

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Page 1
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement.
Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Usardi A, Ahmed SF, Bufo R, Choplin T, De Filippo G, Devernois G, Eggermann T, Elli FM, Freson K, García Ramirez A, Germain-Lee EL, Groussin L, Hamdy N, Hanna P, Hiort O, Jüppner H, Kamenický P, Knight N, Kottler ML, Le Norcy E, Lecumberri B, Levine MA, Mäkitie O, Martin R, Martos-Moreno GÁ, Minagawa M, Murray P, Pereda A, Pignolo R, Rejnmark L, Rodado R, Rothenbuhler A, Saraff V, Shoemaker AH, Shore EM, Silve C, Turan S, Woods P, Zillikens MC, Perez de Nanclares G, Linglart A. Mantovani G, et al. Among authors: perez de nanclares g. Nat Rev Endocrinol. 2018 Aug;14(8):476-500. doi: 10.1038/s41574-018-0042-0. Nat Rev Endocrinol. 2018. PMID: 29959430 Free PMC article. Review.
Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients.
Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Ahmed SF, Bufo R, Choplin T, De Filippo G, Devernois G, Eggermann T, Elli FM, Garcia Ramirez A, Germain-Lee EL, Groussin L, Hamdy NAT, Hanna P, Hiort O, Jüppner H, Kamenický P, Knight N, Le Norcy E, Lecumberri B, Levine MA, Mäkitie O, Martin R, Martos-Moreno GÁ, Minagawa M, Murray P, Pereda A, Pignolo R, Rejnmark L, Rodado R, Rothenbuhler A, Saraff V, Shoemaker AH, Shore EM, Silve C, Turan S, Woods P, Zillikens MC, Perez de Nanclares G, Linglart A. Mantovani G, et al. Among authors: perez de nanclares g. Horm Res Paediatr. 2020;93(3):182-196. doi: 10.1159/000508985. Epub 2020 Aug 5. Horm Res Paediatr. 2020. PMID: 32756064 Free PMC article. Review.
Congenital cutaneous ossification.
Gomes TF, Kieselová K, Santiago F, Cardoso JC, Cunha F, Sousa SB, Perez de Nanclares G. Gomes TF, et al. Among authors: perez de nanclares g. J Paediatr Child Health. 2022 Jul;58(7):1262-1264. doi: 10.1111/jpc.15814. Epub 2021 Oct 27. J Paediatr Child Health. 2022. PMID: 34706128 No abstract available.
Impaired proteostasis in rare neurological diseases.
Osinalde N, Duarri A, Ramirez J, Barrio R, Perez de Nanclares G, Mayor U. Osinalde N, et al. Among authors: perez de nanclares g. Semin Cell Dev Biol. 2019 Sep;93:164-177. doi: 10.1016/j.semcdb.2018.10.007. Epub 2018 Nov 3. Semin Cell Dev Biol. 2019. PMID: 30355526 Review.
Nutrition recommendations for patients with pseudohypoparathyroidism.
Miñones-Suarez L, Pérez de Nanclares G, Marín-Del Barrio S, Alcázar Villar MJ, de Sotto-Esteban D, Mogas E, Rey Cordo L, Riaño-Galán I, Lumbreras Fernández J, Leis R; en representación del Grupo de Trabajo de Metabolismo Calcio-Fósforo de la Sociedad Española de Endocrinología Pediátrica; de la Sociedad Española de Nefrología Pediátrica y del Comité de Nutrición y Lactancia Materna de la AEP. Miñones-Suarez L, et al. Among authors: perez de nanclares g. An Pediatr (Engl Ed). 2023 Aug;99(2):129-135. doi: 10.1016/j.anpede.2023.05.007. Epub 2023 Jul 21. An Pediatr (Engl Ed). 2023. PMID: 37481364 Free article.
Brachydactyly E: isolated or as a feature of a syndrome.
Pereda A, Garin I, Garcia-Barcina M, Gener B, Beristain E, Ibañez AM, Perez de Nanclares G. Pereda A, et al. Among authors: perez de nanclares g. Orphanet J Rare Dis. 2013 Sep 12;8:141. doi: 10.1186/1750-1172-8-141. Orphanet J Rare Dis. 2013. PMID: 24028571 Free PMC article. Review.
Albright's hereditary osteodystrophy: an entity to recognize.
Maduro AI, Pinto Saraiva A, Pimenta Rodrigues O, Marques M, B Sousa S, Malcata A, Perez de Nanclares G, Serra S. Maduro AI, et al. Among authors: perez de nanclares g. Rheumatology (Oxford). 2022 Nov 2;61(11):e356-e357. doi: 10.1093/rheumatology/keac277. Rheumatology (Oxford). 2022. PMID: 35551352 No abstract available.
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci.
Eggermann T, Perez de Nanclares G, Maher ER, Temple IK, Tümer Z, Monk D, Mackay DJ, Grønskov K, Riccio A, Linglart A, Netchine I. Eggermann T, et al. Among authors: perez de nanclares g. Clin Epigenetics. 2015 Nov 14;7:123. doi: 10.1186/s13148-015-0143-8. eCollection 2015. Clin Epigenetics. 2015. PMID: 26583054 Free PMC article. Review.
111 results