HomeLiterature Search
Popular searches
Longitudinal association between executive function and academic achievement in…

Hou(Y),Wu(X),Allen(T),Toledo-Tamula(MA),Mart… J Int Neuropsychol Soc 2023-00-00

...NF1) and plexiform neurofibromas (PNs) and whether age at baseline moderates this relationship. Participants included 88...

Maintaining Engagement in Adults with Neurofibromatosis Type 1 to Use the iCanC…

Buono(FD),Larkin(K),Pham(Q),De Sousa(D),Zemp… Cancers (Basel) 2023-06-16

Neurofibromatosis Type 1 (NF1) is an autosomal dominant genetic condition in which chronic pain is a predominant issue. ...

A standardized imaging and analysis workflow for quantitative evaluation of cut…

Fertitta(L),Coulpier(F),Oubrou(L),Decrouy(X)… PLoS One None

...Nf1-KO mouse model which recapitulates key features of cNFs. In this model, Nf1 inactivation and tdTomato (Tom) reporter...

Neurofibromatosis Type 1 in Ecuador: genotype-phenotype correlations from a cas…

Paz-Cruz(E),Guevara-Ramirez(P),Llamos Panequ… Medwave 2026-01-14

Neurofibromatosis type 1 (NF1) is a multisystemic genetic disorder caused by pathogenic variants in the gene, characteri...

Serial MRIs provide novel insight into natural history of optic pathway gliomas…

Sellmer(L),Farschtschi(S),Marangoni(M),Heran… Orphanet J Rare Dis 2018-00-23

Optic pathway gliomas (OPGs) are present in 20% of children with neurofibromatosis 1 (NF1) but are less frequently obser...

Fatal abdominal hemorrhage following surgery to remove a retroperitoneal MPNST …

Pei(YY),Yang(TT),Zhang(HD),Yu(TS) Medicine (Baltimore) 2024-11-29

Individuals diagnosed with neurofibromatosis type I (NF1) commonly present with neurofibromas, and a subset may progress...

Pain, skin sensations symptoms, and cognitive functioning predictors of health-…

Varni(JW),Nutakki(K),Swigonski(NL) Qual Life Res 2019-04-00

...NF1. Delineating NF1-specific symptoms and cognitive functioning as high-priority predictors from the patient and parent...

Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, de…

Pemov(A),Hansen(NF),Sindiri(S),Patidar(R),Hi… Neuro Oncol 2019-00-05

...NF1) is a tumor-predisposition disorder caused by germline mutations in NF1. NF1 patients have an 8-16% lifetime risk of...

Genomic alterations underlying spinal metastases in pediatric H3K27M-mutant pin…

Fomchenko(EI),Erson-Omay(EZ),Kundishora(AJ),… J Neurosurg Pediatr 2019-10-25

...NF1 that resulted in biallelic NF1 loss. They noted a hypermutated phenotype with increased C>T transitions within the P...

Near-Bloodless Resection of a Giant Hypervascular NF1-Associated Malignant Peri…

Sato(M),Saito(Y),Yuki(A),Hirata(T),Abe(R) Int J Dermatol 2026-07-00

None

Previous 451 452 453 454 455 456 457 458 459 Next Vol. 455 / of 899 页

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com