Doser K, Jepsen J, Kenborg L, Miskowiak K, Albieri V, Dalton S
Orphanet J Rare Dis. 2024; 19(1):441.
PMID: 39609892
PMC: 11603635.
DOI: 10.1186/s13023-024-03454-w.
Miyagishima K, Qiao F, Stasheff S, Nadal-Nicolas F
Vision (Basel). 2024; 8(2).
PMID: 38804352
PMC: 11130890.
DOI: 10.3390/vision8020031.
Agouridis A, Palli N, Karagiorga V, Konsoula A, Markaki L, Spernovasilis N
Children (Basel). 2023; 10(9).
PMID: 37761518
PMC: 10528298.
DOI: 10.3390/children10091556.
Carotenuto M, Messina G, Esposito M, Santoro C, Iacono D, Spruyt K
Front Neurol. 2023; 14:1213430.
PMID: 37538252
PMC: 10394094.
DOI: 10.3389/fneur.2023.1213430.
Pillay-Smiley N, Leach J, Lane A, Hummel T, Fangusaro J, de Blank P
Cancers (Basel). 2023; 15(7).
PMID: 37046770
PMC: 10092996.
DOI: 10.3390/cancers15072109.
Bibliometric analysis of the top 100 most-cited articles in neurofibromatosis.
Alnefaie N, Almutairi O, Alturki A, Bafaquh M
Surg Neurol Int. 2022; 13:282.
PMID: 35855179
PMC: 9282785.
DOI: 10.25259/SNI_114_2022.
Perspectives on adapting a mobile application for pain self-management in neurofibromatosis type 1: results of online focus group discussions with individuals living with neurofibromatosis type 1 and pain management experts.
Grau L, Larkin K, Lalloo C, Stinson J, Zempsky W, Ball S
BMJ Open. 2022; 12(7):e056692.
PMID: 35840301
PMC: 9295671.
DOI: 10.1136/bmjopen-2021-056692.
Determination of Vitamin D Levels in Patients With Neurofibromatosis Type 1 in the Pediatric Age Group.
Santos A, Geller M, Mezitis S, Rubenstein A, Oliveira L, Medeiros Lima D
Clin Pathol. 2022; 13:2632010X20928930.
PMID: 35156025
PMC: 8826272.
DOI: 10.1177/2632010X20928930.
Social behavior in RASopathies and idiopathic autism.
Foy A, Hudock R, Shanley R, Pierpont E
J Neurodev Disord. 2022; 14(1):5.
PMID: 35021989
PMC: 8753327.
DOI: 10.1186/s11689-021-09414-w.
The diagnostic accuracy and prognostic value of OCT for the evaluation of the visual function in children with a brain tumour: A systematic review.
Nuijts M, Imhof S, Veldhuis N, Dekkers C, Schouten-van Meeteren A, Stegeman I
PLoS One. 2021; 16(12):e0261631.
PMID: 34941930
PMC: 8699950.
DOI: 10.1371/journal.pone.0261631.
Predicting pediatric optic pathway glioma progression using advanced magnetic resonance image analysis and machine learning.
Pisapia J, Akbari H, Rozycki M, Thawani J, Storm P, Avery R
Neurooncol Adv. 2020; 2(1):vdaa090.
PMID: 32885166
PMC: 7455885.
DOI: 10.1093/noajnl/vdaa090.
Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRI.
Calvez S, Levy R, Calvez R, Roux C, Grevent D, Purcell Y
AJNR Am J Neuroradiol. 2020; 41(9):1733-1739.
PMID: 32816766
PMC: 7583105.
DOI: 10.3174/ajnr.A6740.
Effect of age and neurofibromatosis type 1 status on white matter integrity in the optic radiations.
de Blank P, Berman J, Prelack M, Sollee J, Lane A, Waldman A
Neurooncol Adv. 2020; 2(Suppl 1):i150-i158.
PMID: 32642741
PMC: 7317057.
DOI: 10.1093/noajnl/vdaa037.
An executive functioning perspective in neurofibromatosis type 1: from ADHD and autism spectrum disorder to research domains.
Smith T, Kaczorowski J, Acosta M
Childs Nerv Syst. 2020; 36(10):2321-2332.
PMID: 32617712
DOI: 10.1007/s00381-020-04745-w.
Late morbidity and mortality in adult survivors of childhood glioma with neurofibromatosis type 1: report from the Childhood Cancer Survivor Study.
de Blank P, Li N, Fisher M, Ullrich N, Bhatia S, Yasui Y
Genet Med. 2020; 22(11):1794-1802.
PMID: 32572180
PMC: 7606750.
DOI: 10.1038/s41436-020-0873-7.
Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?.
Biotteau M, Dejean S, Lelong S, Iannuzzi S, Faure-Marie N, Castelnau P
Front Neurol. 2020; 11:368.
PMID: 32431664
PMC: 7214842.
DOI: 10.3389/fneur.2020.00368.
Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.
Kaczorowski J, Smith T, Shrewsbury A, Thomas L, Knopik V, Acosta M
Behav Genet. 2020; 50(4):191-202.
PMID: 32026187
DOI: 10.1007/s10519-020-09991-x.
Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966.
Bergqvist C, Servy A, Valeyrie-Allanore L, Ferkal S, Combemale P, Wolkenstein P
Orphanet J Rare Dis. 2020; 15(1):37.
PMID: 32014052
PMC: 6998847.
DOI: 10.1186/s13023-020-1310-3.
Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 1 - clinical and neuroimaging findings.
Salman M, Hossain S, Alqublan L, Bunge M, Rozovsky K
Cerebellum Ataxias. 2018; 5:14.
PMID: 30410779
PMC: 6211433.
DOI: 10.1186/s40673-018-0093-y.
Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 2 - a neuroimaging natural history study with clinical correlations.
Salman M, Hossain S, Gorun S, Alqublan L, Bunge M, Rozovsky K
Cerebellum Ataxias. 2018; 5:13.
PMID: 30410778
PMC: 6208104.
DOI: 10.1186/s40673-018-0092-z.