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Hereditary sensory autonomic neuropathy caused by a mutation in dystonin

Annals of neurology, 2012-04, Vol.71 (4), p.569-572

2012

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Hereditary sensory and autonomic neuropathies: types II, III, and IV

Orphanet journal of rare diseases, 2007-10, Vol.2 (1), p.39-39, Article 39

2007

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Familial dysautonomia

Muscle & nerve, 2004-03, Vol.29 (3), p.352-363

Axelrod, Felicia B.

2004

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Pediatric autonomic disorders

Pediatrics (Evanston), 2006-07, Vol.118 (1), p.309

2006

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Olfactory stem cells, a new cellular model for studying molecular mechanisms underlying familial dysautonomia

PloS one, 2010-12, Vol.5 (12), p.e15590-e15590

2010

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Genetic Autonomic Disorders

Seminars in pediatric neurology, 2013-03, Vol.20 (1), p.3-11

Axelrod, Felicia B., MD

2013

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A Rating Scale for the Functional Assessment of Patients with Familial Dysautonomia (Riley Day Syndrome)

The Journal of pediatrics, 2012-12, Vol.161 (6), p.1160-1165

2012

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Hereditary sensory and autonomic neuropathies. Familial dysautonomia and other HSANs

Clinical autonomic research, 2002-05, Vol.12 Suppl 1, p.I2-14

Axelrod, Felicia B

2002

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Renal Transplantation in Familial Dysautonomia: Report of Two Cases and Review of the Literature

Clinical journal of the American Society of Nephrology, 2010-09, Vol.5 (9), p.1676-1680

2010

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Kinetin Improves IKBKAP mRNA Splicing in Patients With Familial Dysautonomia

Pediatric research, 2011-11, Vol.70 (5), p.480-483

2011

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Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?

Brain (London, England : 1878), 2011-11, Vol.134 (11), p.3198-3208

2011

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Neoplasia in Familial Dysautonomia: A 20-Year Review in a Young Patient Population

The Journal of pediatrics, 2009-12, Vol.155 (6), p.934-936

2009

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Normative values of vibratory perception in 530 children, juveniles and adults aged 3–79 years

Journal of the neurological sciences, 1998-08, Vol.159 (2), p.219-225

1998

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Cardiac‐locked bursts of muscle sympathetic nerve activity are absent in familial dysautonomia

The Journal of physiology, 2013-02, Vol.591 (3), p.689-700

2013

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Disturbances in affective touch in hereditary sensory & autonomic neuropathy type III

International journal of psychophysiology, 2014-07, Vol.93 (1), p.56-61

2014

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Cyclic Vomiting Associated With Excessive Dopamine in Riley-day Syndrome

Journal of clinical gastroenterology, 2013-02, Vol.47 (2), p.136-138

2013

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Cardiac sympathetic hypo-innervation in familial dysautonomia

Clinical autonomic research, 2008-06, Vol.18 (3), p.115-119

2008

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Relationship between proprioception at the knee joint and gait ataxia in HSAN III

Movement disorders, 2013-06, Vol.28 (6), p.823-827

2013

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Peripheral Arthropathy in Hereditary Sensory and Autonomic Neuropathy Types III and IV

Journal of pediatric orthopaedics, 2009-01, Vol.29 (1), p.91-97

2009

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Assessing Efficacy of High-Frequency Chest Wall Oscillation in Patients With Familial Dysautonomia

Chest, 2005-11, Vol.128 (5), p.3377-3381

2005

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Obstructive Sleep-Disordered Breathing Is More Common than Central in Mild Familial Dysautonomia

Journal of clinical sleep medicine, 2016-12, Vol.12 (12), p.1607-1614

2016

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Tissue-Specific Expression of a Splicing Mutation in the IKBKAP Gene Causes Familial Dysautonomia

American journal of human genetics, 2001-03, Vol.68 (3), p.598-605

2001

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Genome-wide analysis of familial dysautonomia and kinetin target genes with patient olfactory ecto-mesenchymal stem cells

Human mutation, 2012-03, Vol.33 (3), p.530-540

2012

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Hereditary sensory autonomic neuropathy caused by a mutation in dystonin

Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome

Hereditary sensory and autonomic neuropathies: types II, III, and IV

Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome

Familial dysautonomia

Pediatric autonomic disorders

Olfactory stem cells, a new cellular model for studying molecular mechanisms underlying familial dysautonomia

Genetic Autonomic Disorders

A Rating Scale for the Functional Assessment of Patients with Familial Dysautonomia (Riley Day Syndrome)

Hereditary sensory and autonomic neuropathies. Familial dysautonomia and other HSANs

Renal Transplantation in Familial Dysautonomia: Report of Two Cases and Review of the Literature

Kinetin Improves IKBKAP mRNA Splicing in Patients With Familial Dysautonomia

Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?

Neoplasia in Familial Dysautonomia: A 20-Year Review in a Young Patient Population

Normative values of vibratory perception in 530 children, juveniles and adults aged 3–79 years

Cardiac‐locked bursts of muscle sympathetic nerve activity are absent in familial dysautonomia

Disturbances in affective touch in hereditary sensory & autonomic neuropathy type III

Cyclic Vomiting Associated With Excessive Dopamine in Riley-day Syndrome

Cardiac sympathetic hypo-innervation in familial dysautonomia

Relationship between proprioception at the knee joint and gait ataxia in HSAN III

Peripheral Arthropathy in Hereditary Sensory and Autonomic Neuropathy Types III and IV

Assessing Efficacy of High-Frequency Chest Wall Oscillation in Patients With Familial Dysautonomia

Obstructive Sleep-Disordered Breathing Is More Common than Central in Mild Familial Dysautonomia

Tissue-Specific Expression of a Splicing Mutation in the IKBKAP Gene Causes Familial Dysautonomia

Genome-wide analysis of familial dysautonomia and kinetin target genes with patient olfactory ecto-mesenchymal stem cells

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