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1. Associations of meningioma molecular subgroup and tumor recurrence. Issue 5 (17th October 2020)

2. Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: Expansion of the facial and neuroimaging features. Issue 7 (3rd April 2014)

3. Cross-platform analysis reveals cellular and molecular landscape of glioblastoma invasion. Issue 3 (28th July 2022)

4. DISP-09. THE GENOMIC PROFILES AND CLINICAL MANIFESTATIONS OF MENINGIOMAS VARY AMONGST DIFFERENT RACES. (14th November 2022)

5. EPCO-40. INFRATENTORIAL NF2 MUTANT SPORADIC MENINGIOMAS DIFFER FROM THOSE IN SUPRATENTORIAL LOCATIONS AND ARE MORE BENIGN. (14th November 2022)

7. GENE-56. MENINGIOMA GENOMIC SUBGROUP AS A PREDICTOR OF POST-OPERATIVE PATIENT OUTCOMES: IMPLICATIONS FOR TREATMENT AND FOLLOW-UP. (11th November 2019)

8. Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome. Issue 2 (4th February 2018)

9. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus. (16th November 2020)

10. Longitudinal analysis of treatment-induced genomic alterations in gliomas. Issue 1 (December 2017)