Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1995 2
2008 1
2010 2
2011 1
2012 4
2013 7
2014 5
2015 2
2016 6
2017 5
2018 4
2019 2
2020 3
2021 0
Text availability
Article attribute
Article type
Publication date

Search Results

40 results
Results by year
Filters applied: . Clear all
Page 1
DIAGNOSIS OF ENDOCRINE DISEASE: Congenital hypothyroidism: update and perspectives.
Peters C, van Trotsenburg ASP, Schoenmakers N. Peters C, et al. Among authors: schoenmakers n. Eur J Endocrinol. 2018 Dec 1;179(6):R297-R317. doi: 10.1530/EJE-18-0383. Eur J Endocrinol. 2018. PMID: 30324792 Review.
Recent advances in central congenital hypothyroidism.
Schoenmakers N, Alatzoglou KS, Chatterjee VK, Dattani MT. Schoenmakers N, et al. J Endocrinol. 2015 Dec;227(3):R51-71. doi: 10.1530/JOE-15-0341. Epub 2015 Sep 28. J Endocrinol. 2015. PMID: 26416826 Free PMC article. Review.
2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism.
Persani L, Brabant G, Dattani M, Bonomi M, Feldt-Rasmussen U, Fliers E, Gruters A, Maiter D, Schoenmakers N, van Trotsenburg ASP. Persani L, et al. Among authors: schoenmakers n. Eur Thyroid J. 2018 Oct;7(5):225-237. doi: 10.1159/000491388. Epub 2018 Jul 19. Eur Thyroid J. 2018. PMID: 30374425 Free PMC article.
Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia.
Zdraveska N, Kocova M, Nicholas AK, Anastasovska V, Schoenmakers N. Zdraveska N, et al. Among authors: schoenmakers n. Front Endocrinol (Lausanne). 2020 Jul 14;11:413. doi: 10.3389/fendo.2020.00413. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32765423 Free PMC article.
IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction.
Joustra SD, Roelfsema F, van Trotsenburg ASP, Schneider HJ, Kosilek RP, Kroon HM, Logan JG, Butterfield NC, Zhou X, Toufaily C, Bak B, Turgeon MO, Brûlé E, Steyn FJ, Gurnell M, Koulouri O, Le Tissier P, Fontanaud P, Duncan Bassett JH, Williams GR, Oostdijk W, Wit JM, Pereira AM, Biermasz NR, Bernard DJ, Schoenmakers N. Joustra SD, et al. Among authors: schoenmakers n. J Clin Endocrinol Metab. 2020 Mar 1;105(3):e70-84. doi: 10.1210/clinem/dgz093. J Clin Endocrinol Metab. 2020. PMID: 31650157 Free PMC article.
Response to Letter to the Editor: "IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction".
Joustra SD, Roelfsema F, van Trotsenburg ASP, Schneider HJ, Kosilek RP, Kroon HM, Logan JG, Butterfield NC, Zhou X, Toufaily C, Bak B, Turgeon MO, Brûlé E, Steyn FJ, Gurnell M, Koulouri O, Le Tissier P, Fontanaud P, Bassett JHD, Williams GR, Oostdijk W, Wit JM, Pereira AM, Biermasz NR, Bernard DJ, Schoenmakers N. Joustra SD, et al. Among authors: schoenmakers n. J Clin Endocrinol Metab. 2020 Jun 1;105(6):e2315-6. doi: 10.1210/clinem/dgaa147. J Clin Endocrinol Metab. 2020. PMID: 32211768 Free PMC article. No abstract available.
Haploinsufficiency of NKX2-1 in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction.
Prasad R, Nicholas AK, Schoenmakers N, Barton J. Prasad R, et al. Among authors: schoenmakers n. Horm Res Paediatr. 2019;92(5):340-344. doi: 10.1159/000503683. Epub 2019 Nov 8. Horm Res Paediatr. 2019. PMID: 31707387 Free article.
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
Cangul H, Liao XH, Schoenmakers E, Kero J, Barone S, Srichomkwun P, Iwayama H, Serra EG, Saglam H, Eren E, Tarim O, Nicholas AK, Zvetkova I, Anderson CA, Frankl FEK, Boelaert K, Ojaniemi M, Jääskeläinen J, Patyra K, Löf C, Williams ED; UK10K Consortium, Soleimani M, Barrett T, Maher ER, Chatterjee VK, Refetoff S, Schoenmakers N. Cangul H, et al. Among authors: schoenmakers n. JCI Insight. 2018 Oct 18;3(20):e99631. doi: 10.1172/jci.insight.99631. JCI Insight. 2018. PMID: 30333321 Free PMC article.
DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom.
Peters C, Nicholas AK, Schoenmakers E, Lyons G, Langham S, Serra EG, Sebire NJ, Muzza M, Fugazzola L, Schoenmakers N. Peters C, et al. Among authors: schoenmakers n. Thyroid. 2019 Jun;29(6):790-801. doi: 10.1089/thy.2018.0587. Thyroid. 2019. PMID: 31044655 Free PMC article.
Semantic prioritization of novel causative genomic variants.
Boudellioua I, Mahamad Razali RB, Kulmanov M, Hashish Y, Bajic VB, Goncalves-Serra E, Schoenmakers N, Gkoutos GV, Schofield PN, Hoehndorf R. Boudellioua I, et al. Among authors: schoenmakers n. PLoS Comput Biol. 2017 Apr 17;13(4):e1005500. doi: 10.1371/journal.pcbi.1005500. eCollection 2017 Apr. PLoS Comput Biol. 2017. PMID: 28414800 Free PMC article.
40 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page