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Employment (2)

Gillette Children's Specialty Healthcare: Saint Paul, MN, US

2016-07 to present | Program Director (Neuromuscular)
Employment
Source: Self-asserted source
Randal Richardson

Gillette Children's Specialty Healthcare: Saint Paul, MN, US

2013 to present | Staff Neurologist (Neurology)
Employment
Source: Self-asserted source
Randal Richardson

Works (17)

Cost-effectiveness of Nusinersen for Spinal Muscular Atrophy.

JAMA pediatrics
2018-07 | Journal article
Contributors: Richardson RC
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

A common COL6A1 deep-intronic pseudo-exon inserting mutation causes a distinct phenotype of Ullrich congenital muscular dystrophy.

World Muscle Society Conference
2017-10 | Conference poster
Source: Self-asserted source
Randal Richardson

Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia.

Orphanet journal of rare diseases
2017-06 | Journal article
Contributors: Zambonin JL; Bellomo A; Ben-Pazi H; Everman DB; Frazer LM; Geraghty MT; Harper AD; Jones JR; Kamien B; Kernohan K et al.
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Characterization of pulmonary function in 10-18 year old patients with Duchenne muscular dystrophy.

Neuromuscular disorders : NMD
2017-01 | Journal article
Contributors: Meier T; Rummey C; Leinonen M; Spagnolo P; Mayer OH; Buyse GM; DELOS Study Group
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy.

Neuromuscular disorders : NMD
2016-05 | Journal article
Contributors: McDonald CM; Meier T; Voit T; Schara U; Straathof CS; D'Angelo MG; Bernert G; Cuisset JM; Finkel RS; Goemans N et al.
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy.

Human mutation
2014-11 | Journal article
Contributors: Lee JR; Srour M; Kim D; Hamdan FF; Lim SH; Brunel-Guitton C; Décarie JC; Rossignol E; Mitchell GA; Schreiber A et al.
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Truncating CLCN1 mutations in myotonia congenita: variable patterns of inheritance.

Muscle & nerve
2013-09 | Journal article
Contributors: Richardson RC; Tarleton JC; Bird TD; Gospe SM
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Isolated lower brachial plexus (Klumpke) palsy with compound arm presentation: case report.

The Journal of hand surgery
2013-06 | Journal article
Contributors: Buchanan EP; Richardson R; Tse R
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutation.

Vascular medicine (London, England)
2011-10 | Journal article
Contributors: Skeik N; Rooke TW; Davis MD; Davis DM; Kalsi H; Kurth I; Richardson RC
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Variable heritability of truncating CLCN1 mutations in myotonia congenita

American Academy of Neurology Meeting
2009-04 | Conference poster
Source: Self-asserted source
Randal Richardson

Unilateral myokymia of the tongue after radiation therapy for cervical nodal melanoma.

Journal of clinical neuromuscular disease
2009-03 | Journal article
Contributors: Richardson RC; Weiss MD
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Neurologic Disorders

Practical Guide to the Care of the Pediatric Patient: Practical Guide Series (2nd Edition)
2007-10-19 | Book chapter
Part of ISBN: 0323036708
Source: Self-asserted source
Randal Richardson

Comparison of accidental and nonaccidental traumatic head injury in children on noncontrast computed tomography.

Pediatrics
2006-08 | Journal article
Contributors: Tung GA; Kumar M; Richardson RC; Jenny C; Brown WD
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Inhibitory network properties shaping the light evoked responses of cat alpha retinal ganglion cells.

Visual neuroscience
2003-07 | Journal article
Contributors: O'Brien BJ; Richardson RC; Berson DM
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Intrinsic physiological properties of cat retinal ganglion cells.

The Journal of physiology
2002-02 | Journal article
Contributors: O'Brien BJ; Isayama T; Richardson R; Berson DM
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Developmental changes in seizure susceptibility during ethanol withdrawal.

Alcohol (Fayetteville, N.Y.)
1999-05 | Journal article
Contributors: Acheson SK; Richardson R; Swartzwelder HS
Source: Self-asserted source
Randal Richardson via Europe PubMed Central

Developmental differences in the acquisition of tolerance to ethanol.

Alcohol (Fayetteville, N.Y.)
1998-05 | Journal article
PMID: 9590516
Contributors: Swartzwelder HS; Richardson RC; Markwiese-Foerch B; Wilson WA; Little PJ
Source: Self-asserted source
Randal Richardson via Europe PubMed Central