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Extreme mortality and reproductive failure of common murres resulting from the northeast Pacific marine heatwave of 2014-2016

PloS one, 2020-01, Vol.15 (1), p.e0226087-e0226087

2020

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Natural history of Ullrich congenital muscular dystrophy

Neurology, 2009-07, Vol.73 (1), p.25-31

2009

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Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7

Neurology, 2010-05, Vol.74 (19), p.1517-1523

2010

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Congenital myopathies – Clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom

Neuromuscular disorders : NMD, 2013-03, Vol.23 (3), p.195-205

2013

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Endovascular management for peripheral arterial trauma: The new norm?

Injury, 2017-05, Vol.48 (5), p.1025-1030

2017

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8.4 Rational Use of Antipsychotic Drugs and Mood Stabilizers in Youth With Aggression in Autism and Bipolar Disorder

Journal of the American Academy of Child and Adolescent Psychiatry, 2016-10, Vol.55 (10), p.S99-S99

Robb, Adelaide S., MD

2016

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Practical Pediatric Psychopharmacology for the Primary Care Practitioner and Early Career Psychiatrist

Journal of the American Academy of Child and Adolescent Psychiatry, 2016-10, Vol.55 (10), p.S98-S98

Robb, Adelaide S., MD

2016

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SSRI use during pregnancy

Seminars in perinatology, 2015-11, Vol.39 (7), p.545-547

2015

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RYR1 -related congenital myopathy with fatigable weakness, responding to pyridostigimine

Neuromuscular disorders : NMD, 2014-08, Vol.24 (8), p.707-712

2014

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Congenital Myasthenic Syndromes in childhood: Diagnostic and management challenges

Journal of neuroimmunology, 2008-09, Vol.201, p.6-12

2008

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Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Neurology, 2005-12, Vol.65 (12), p.1930-1935

2005

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Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomy

Neuromuscular disorders : NMD, 2014-01, Vol.24 (1), p.25-30

2014

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Congenital fibre type disproportion associated with mutations in the tropomyosin 3 ( TPM3 ) gene mimicking congenital myasthenia

Neuromuscular disorders : NMD, 2010-12, Vol.20 (12), p.796-800

2010

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Mercury concentrations in breast feathers of three upper trophic level marine predators from the western Aleutian Islands, Alaska

Marine pollution bulletin, 2014-05, Vol.82 (1-2), p.189-193

2014

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Effects of Survey Methods on Burrowing Owl Behaviors

The Journal of wildlife management, 2011-04, Vol.75 (3), p.525-530

2011

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Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008

Neuromuscular disorders : NMD, 2012-06, Vol.22 (6), p.522-527

2012

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SEPN1-related myopathies: clinical course in a large cohort of patients

Neurology, 2011-06, Vol.76 (24), p.2073-2078

2011

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Diagnostic value of muscle MRI in rare congenital myopathies and collagen related muscular dystrophies

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S41-S42

2017

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The Whitlam government and the Republic of Korea: responding to human rights challenges in foreign policy

International history review, 2023-03, Vol.45 (2), p.372-390

Robb, Kevin S.

2023

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4.3 EFFECT OF LURASIDONE ON BODY WEIGHT AND LABORATORY PARAMETERS IN ADOLESCENT PATIENTS WITH SCHIZOPHRENIA: RESULTS FROM A 6-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY

Journal of the American Academy of Child and Adolescent Psychiatry, 2016-10, Vol.55 (10), p.S163-S163

2016

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Analysis of an adult Duchenne muscular dystrophy population

QJM : An International Journal of Medicine, 2005-10, Vol.98 (10), p.729-736

2005

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4.62 A SIX-MONTH OPEN-LABEL EXTENSION STUDY OF VORTIOXETINE IN PEDIATRIC PATIENTS

Journal of the American Academy of Child and Adolescent Psychiatry, 2016-10, Vol.55 (10), p.S183-S183

2016

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Dopamine Transporter Genotype and Methylphenidate Dose Response in Children with ADHD

Neuropsychopharmacology (New York, N.Y.), 2005-07, Vol.30 (7), p.1374-1382

2005

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Clonidine for Attention-Deficit/Hyperactivity Disorder: II. ECG Changes and Adverse Events Analysis

Journal of the American Academy of Child and Adolescent Psychiatry, 2008-02, Vol.47 (2), p.189-198

2008

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Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes

Neurology, 2003-09, Vol.61 (6), p.826-828

2003

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Extreme mortality and reproductive failure of common murres resulting from the northeast Pacific marine heatwave of 2014-2016

Natural history of Ullrich congenital muscular dystrophy

Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7

Congenital myopathies – Clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom

Endovascular management for peripheral arterial trauma: The new norm?

8.4 Rational Use of Antipsychotic Drugs and Mood Stabilizers in Youth With Aggression in Autism and Bipolar Disorder

Practical Pediatric Psychopharmacology for the Primary Care Practitioner and Early Career Psychiatrist

SSRI use during pregnancy

RYR1 -related congenital myopathy with fatigable weakness, responding to pyridostigimine

Congenital Myasthenic Syndromes in childhood: Diagnostic and management challenges

Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomy

Congenital fibre type disproportion associated with mutations in the tropomyosin 3 ( TPM3 ) gene mimicking congenital myasthenia

Mercury concentrations in breast feathers of three upper trophic level marine predators from the western Aleutian Islands, Alaska

Effects of Survey Methods on Burrowing Owl Behaviors

Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008

SEPN1-related myopathies: clinical course in a large cohort of patients

Diagnostic value of muscle MRI in rare congenital myopathies and collagen related muscular dystrophies

The Whitlam government and the Republic of Korea: responding to human rights challenges in foreign policy

4.3 EFFECT OF LURASIDONE ON BODY WEIGHT AND LABORATORY PARAMETERS IN ADOLESCENT PATIENTS WITH SCHIZOPHRENIA: RESULTS FROM A 6-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY

Analysis of an adult Duchenne muscular dystrophy population

4.62 A SIX-MONTH OPEN-LABEL EXTENSION STUDY OF VORTIOXETINE IN PEDIATRIC PATIENTS

Dopamine Transporter Genotype and Methylphenidate Dose Response in Children with ADHD

Clonidine for Attention-Deficit/Hyperactivity Disorder: II. ECG Changes and Adverse Events Analysis

Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes

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