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Evaluation of magnetic resonance imaging-based radiomics characteristics for di…

Ristow(I),Madesta(F),Well(L),Shenas(F),Wrigh… Neuro Oncol 2022-00-03

...NF1 patients. MRI was performed at 3T in 36 NF1 patients (20 male; age: 31 ± 11 years). Segmentation of 117 BPNSTs, 17 M...

Exceptional response to everolimus in an NF1-deficient recurrent endometrioid a…

Machulak(M),Zwierzchowska(M),Łysak(K),Kośmid… Front Oncol None

...NF1 (neurofibromin 1) gene. Based on the molecular profile of the tumor, the patient was qualified for off-label targete...

Morphological Differences in the Vertebrae of Scoliosis Secondary to Neurofibro…

Hu(Zongshan),Liu(Zhen),Qiu(Yong),Xu(Leilei),… Spine (Phila Pa 1976) 0000-00-00

...NF1-S) with and without paraspinal neurofibromas and to identify the relationship between paraspinal neurofibromas and v...

A randomized placebo-controlled lovastatin trial for neurobehavioral function i…

Bearden(Carrie E),Hellemann(Gerhard S),Rosse… Ann Clin Transl Neurol 2016-04-15

...NF1.,Forty-four NF1 patients (mean age 25.7+/-11.6 years; 64% female) were randomly assigned to 14 weeks of lovastatin (...

Management of congenital pseudarthrosis of the tibia with the Ilizarov method i…

Borzunov(Dmitry Y),Chevardin(Alexander Y),Mi… Int Orthop 2016-11-01

...NF1) or CPT of idiopathic origin in paediatric patients.,We studied the outcomes of 28 children that were treated for CP...

Loss of H3K27me3 Expression Is a Highly Sensitive Marker for Sporadic and Radia…

Prieto-Granada(Carlos N),Wiesner(Thomas),Mes… Am J Surg Pathol 2016-08-02

Most malignant peripheral nerve sheath tumors (MPNSTs) exhibit combined inactivation of NF1, CDKN2A, and polycomb repres...

Systematic MRI in NF1 children under six years of age for the diagnosis of opti…

Blanchard(Gaelle),Lafforgue(Marie-Pierre),Li… Eur J Paediatr Neurol 2016-09-26

Optic pathway glioma (OPG) is the most common central nervous system tumor in children with neurofibromatosis type 1 (NF...

Autism Spectrum Disorder Symptom Profiles in Fragile X Syndrome, Angelman Syndr…

Lubbers(K),Hiralal(KR),Dieleman(GC),Hagenaar… J Autism Dev Disord 2024-10-12

...NF1) are monogenic disorders with high a prevalence of ASD symptomatology. This study aimed to identify ASD symptom prof...

Irritability in Children with Rasopathies, Insights into Emotional Dysregulatio…

Serur(Y),Fuhrman(N),Russo(O),Green(T) Res Sq 2024-12-19

Rasopathies, including Noonan Syndrome (NS) and Neurofibromatosis type 1 (NF1), are developmental disorders caused by ge...

Clinicopathological significance of mutation profile detected by next generatio…

Akın(D),Kahraman Çeti N(N),Erdoğdu(İH),Öztür… Pathol Res Pract 2024-08-00

...NF1 mutation(p=0.001), while the liver exhibited a significant BRAF mutation(p=0.000). NF1-TP53, PTEN-TP53 and NF1-PTEN ...

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