Page last updated: 2024-08-23

s-adenosylmethionine and Bulbar Palsy

s-adenosylmethionine has been researched along with Bulbar Palsy in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abrams, AJ; Al-Odaib, A; Antony, J; Baxter, PS; Brandner, S; Broomfield, A; Burns, J; Carpenter, K; Christodoulou, J; Clayton, P; Farrell, MO; Foley, AR; Forman, E; Gold, W; Gonzalez, MA; Hargreaves, I; Horvath, R; Houlden, H; Hughes, I; Jungbluth, H; King, MD; Land, JM; Lek, M; Lim, MJ; Lin, JP; Manzur, AY; Mathew, AA; Matsubara, K; McCullagh, BG; McGarvey, ML; Megarbane, A; Menezes, MP; Muntoni, F; Ng, J; O'Brien, K; O'Byrne, JJ; Olpin, S; Oppenheim, M; Ouvrier, RA; Pandraud, A; Phadke, R; Prasad, M; Rahman, S; Reilly, MM; Scherer, SS; Scoto, M; Shah, AH; Straub, V; Sugano, K; Urtizberea, JA; Wang, MX; Webster, R; Yonezawa, A; Züchner, S	1

Studies

Abrams, AJ; Al-Odaib, A; Antony, J; Baxter, PS; Brandner, S; Broomfield, A; Burns, J; Carpenter, K; Christodoulou, J; Clayton, P; Farrell, MO; Foley, AR; Forman, E; Gold, W; Gonzalez, MA; Hargreaves, I; Horvath, R; Houlden, H; Hughes, I; Jungbluth, H; King, MD; Land, JM; Lek, M; Lim, MJ; Lin, JP; Manzur, AY; Mathew, AA; Matsubara, K; McCullagh, BG; McGarvey, ML; Megarbane, A; Menezes, MP; Muntoni, F; Ng, J; O'Brien, K; O'Byrne, JJ; Olpin, S; Oppenheim, M; Ouvrier, RA; Pandraud, A; Phadke, R; Prasad, M; Rahman, S; Reilly, MM; Scherer, SS; Scoto, M; Shah, AH; Straub, V; Sugano, K; Urtizberea, JA; Wang, MX; Webster, R; Yonezawa, A; Züchner, S

Other Studies

1 other study(ies) available for s-adenosylmethionine and Bulbar Palsy

Article	Year
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain : a journal of neurology, 2014, Volume: 137, Issue:Pt 1 Topics: Adolescent; Brain; Bulbar Palsy, Progressive; Carnitine; Child; Child, Preschool; Exome; Female; Genotype; Hearing Loss, Sensorineural; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Microarray Analysis; Motor Neuron Disease; Mutation; Neurologic Examination; Pedigree; Receptors, G-Protein-Coupled; Riboflavin; RNA; Sequence Analysis, DNA; Sural Nerve; Vitamins; Young Adult	2014

Article

Year

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.

Brain : a journal of neurology, 2014, Volume: 137, Issue:Pt 1

Topics: Adolescent; Brain; Bulbar Palsy, Progressive; Carnitine; Child; Child, Preschool; Exome; Female; Genotype; Hearing Loss, Sensorineural; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Microarray Analysis; Motor Neuron Disease; Mutation; Neurologic Examination; Pedigree; Receptors, G-Protein-Coupled; Riboflavin; RNA; Sequence Analysis, DNA; Sural Nerve; Vitamins; Young Adult

2014