proline and Benign Cerebellar Neoplasms

proline has been researched along with Benign Cerebellar Neoplasms in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (50.00)	2.80

Authors

Authors	Studies
Alam, MS; Calhoun, B; Haldar, K; Liu, F; Lu, X; Sun, M; Wang, X; Zhang, C	1
Dornhoffer, J; Hartzell, LD; McKelvey, KD; Van Hemert, RL	1

Other Studies

2 other study(ies) available for proline and Benign Cerebellar Neoplasms

Article	Year
Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing. BMC medical genetics, 2020, 02-27, Volume: 21, Issue:1 Topics: Adrenal Gland Neoplasms; Cerebellar Neoplasms; Child; Child, Preschool; Family; Female; Frameshift Mutation; Germ-Line Mutation; Hemangioblastoma; Humans; Male; Middle Aged; Neoplasms, Multiple Primary; Pedigree; Pheochromocytoma; Proline; Retinal Neoplasms; RNA Splicing; Silent Mutation; Spinal Neoplasms; von Hippel-Lindau Disease; Von Hippel-Lindau Tumor Suppressor Protein	2020
Cerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation. The international tinnitus journal, 2008, Volume: 14, Issue:2 Topics: Alleles; Amino Acid Substitution; Base Sequence; Cerebellar Neoplasms; Cerebellopontine Angle; Chromosome Deletion; Codon; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Neoplasms, Multiple Primary; Neuroma, Acoustic; Paraganglioma; Proline; Radiography; Radiosurgery; Succinate Dehydrogenase	2008

Article

Year

Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing.

BMC medical genetics, 2020, 02-27, Volume: 21, Issue:1

Topics: Adrenal Gland Neoplasms; Cerebellar Neoplasms; Child; Child, Preschool; Family; Female; Frameshift Mutation; Germ-Line Mutation; Hemangioblastoma; Humans; Male; Middle Aged; Neoplasms, Multiple Primary; Pedigree; Pheochromocytoma; Proline; Retinal Neoplasms; RNA Splicing; Silent Mutation; Spinal Neoplasms; von Hippel-Lindau Disease; Von Hippel-Lindau Tumor Suppressor Protein

2020

Cerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation.

The international tinnitus journal, 2008, Volume: 14, Issue:2

Topics: Alleles; Amino Acid Substitution; Base Sequence; Cerebellar Neoplasms; Cerebellopontine Angle; Chromosome Deletion; Codon; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Neoplasms, Multiple Primary; Neuroma, Acoustic; Paraganglioma; Proline; Radiography; Radiosurgery; Succinate Dehydrogenase

2008