Suchergebnisse - "Barohn, Richard"

1

The history of acetylcholinesterase inhibitors in the treatment of myasthenia gravis

von: Katz, Natalie K.

2021transfer abstract, in: Phallus Preservation for Locally Advanced Proximal Primary Urethral Carcinoma: Technique and Outcomes

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2

Inclusion Body Myositis

von: Dimachkie, Mazen M.

2012, in: Current neurology and neuroscience reports

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3

Guillain-Barré Syndrome

von: Dimachkie, Mazen M.

2013, in: Current treatment options in neurology

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4

Chronic Inflammatory Demyelinating Polyneuropathy

von: Dimachkie, Mazen M.

2013, in: Current treatment options in neurology

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5

Lingual--Alveolar Contact Pressure during speech in Amyotrophic Lateral Sclerosis: preliminary findings.(Research Article)

von: Knollhoff, Stephanie

2017, in: Journal of speech, language, and hearing research

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6

Inclusion Body Myositis: Update on Pathogenesis and Treatment

von: Naddaf, Elie

2018, in: NeuroRX

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7

Congenital Myasthenic Syndromes: a Clinical and Treatment Approach

von: Farmakidis, Constantine

2018, in: Current treatment options in neurology

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8

LRP4 antibody testing in myasthenia gravis

von: Racke, Michael K.

2022, in: Decomposition of polycarbonate/acrylonitrile-butadiene-styrene blends in e-waste packaging resin and recovery of debrominated carbon materials by supercritical water oxidation process

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9

Update on Inclusion Body Myositis

von: Jabari, Duaa

2018, in: Current rheumatology reports

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10

Using automated electronic medical record data extraction to model ALS survival and progression

von: Karanevich, Alex G.

2018, in: BMC neurology

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11

Preliminary clinical efficacy and safety of BMN 701, GILT-tagged recombinant human acid alpha glucosidase (rhGAA), in late-onset Pompe disease: results of an extension study

von: Byrne, Barry

2014, in: Measles transmission during a large outbreak in California

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12

Progress report on development of classification criteria for adult and juvenile idiopathic inflammatory myopathies

von: Pilkington, Clarissa

2014, in: Pediatric rheumatology

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13

A Bayesian comparative effectiveness trial in action: developing a platform for multisite study adaptive randomization

von: Brown, Alexandra R.

2016, in: Trials

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14

A study on the safety and efficacy of reveglucosidase alfa in patients with late-onset Pompe disease

von: Byrne, Barry J.

2017, in: Orphanet journal of rare diseases

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15

Disease course and therapeutic approach in dermatomyositis: A four-center retrospective study of 100 patients

von: Johnson, Nicholas E.

2015, in: Sperm competition in golden cuttlefish

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16

NEO1 and NEO-EXT studies: Long-term safety of repeat avalglucosidase alfa dosing for 4.5 years in late-onset Pompe disease patients

von: Pena, Loren

2019, in: Molecular genetics and metabolism

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17

A phase 4 prospective study in patients with adult Pompe disease treated with alglucosidase alfa

von: Thurberg, Beth L.

2015, in: Measles transmission during a large outbreak in California

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18

NEO1/NEO-EXT studies: Long-term muscle quantitative magnetic resonance imaging and functional efficacy in adults with late-onset Pompe disease (LOPD) on avalglucosidase alfa treatment

von: Byrne, Barry

2023, in: Molecular genetics and metabolism

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19

NEO1 and NEO-EXT studies: Long-term safety and exploratory efficacy of repeat avalglucosidase alfa dosing for 5.5 years in late-onset Pompe disease patients

von: Dimachkie, Mazen M.

2020, in: Measles transmission during a large outbreak in California

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20

Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose study

von: Pena, Loren D.M.

2019, in: Sperm competition in golden cuttlefish

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