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Results by year

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

Year Number of Results
1970 1
2000 1
2001 2
2002 1
2003 3
2005 1
2006 1
2007 2
2008 1
2012 1
2014 1
2015 2
2016 1
2017 1
2018 5
2019 3
2020 2
2021 2
2022 6
2023 1
2024 0

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35 results

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Page 1
Thrombocytopenia: the good, the bad and the ugly.
Ashworth I, Thielemans L, Chevassut T. Ashworth I, et al. Among authors: thielemans l. Clin Med (Lond). 2022 May;22(3):214-217. doi: 10.7861/clinmed.2022-0146. Clin Med (Lond). 2022. PMID: 35584828 Free PMC article.
Contribution of genetic factors to high rates of neonatal hyperbilirubinaemia on the Thailand-Myanmar border.
Bancone G, Gornsawun G, Peerawaranun P, Penpitchaporn P, Paw MK, Poe DD, Win D, Cicelia N, Mukaka M, Archasuksan L, Thielemans L, Nosten F, White NJ, McGready R, Carrara VI. Bancone G, et al. Among authors: thielemans l. PLOS Glob Public Health. 2022 Jun 17;2(6):e0000475. doi: 10.1371/journal.pgph.0000475. eCollection 2022. PLOS Glob Public Health. 2022. PMID: 36962413 Free PMC article.
Hierarchical Bayesian modelling of disease progression to inform clinical trial design in centronuclear myopathy.
Fouarge E, Monseur A, Boulanger B, Annoussamy M, Seferian AM, De Lucia S, Lilien C, Thielemans L, Paradis K, Cowling BS, Freitag C, Carlin BP, Servais L; NatHis-MTM Study Group. Fouarge E, et al. Among authors: thielemans l. Orphanet J Rare Dis. 2021 Jan 6;16(1):3. doi: 10.1186/s13023-020-01663-7. Orphanet J Rare Dis. 2021. PMID: 33407688 Free PMC article.
Extreme neonatal hyperbilirubinaemia in refugee and migrant populations: retrospective cohort.
Wouda EMN, Thielemans L, Darakamon MC, Nge AA, Say W, Khing S, Hanboonkunupakarn B, Ngerseng T, Landier J, van Rheenen PF, Turner C, Nosten F, McGready R, Carrara VI. Wouda EMN, et al. Among authors: thielemans l. BMJ Paediatr Open. 2020 May 28;4(1):e000641. doi: 10.1136/bmjpo-2020-000641. eCollection 2020. BMJ Paediatr Open. 2020. PMID: 32537522 Free PMC article.
An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.
Vander Stichele G, Durr A, Yoon G, Schüle R, Blackstone C, Esposito G, Buffel C, Oliveira I, Freitag C, van Rooijen S, Hoffmann S, Thielemans L, Cowling BS. Vander Stichele G, et al. Among authors: thielemans l. BMC Neurol. 2022 Mar 24;22(1):115. doi: 10.1186/s12883-022-02595-4. BMC Neurol. 2022. PMID: 35331153 Free PMC article.
35 results