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Hereditary Neuropathy Foundation Company Profile

14:47 EDT 19th September 2019 | BioPortfolio

Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization whose mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth disease (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and support research that will lead to treatments and cures. HNF and partner organization Hannah’s Hope Fund co-sponsor the Global Registry for Inherited Neuropathies (GRIN) to collect clinical and genetic information on patients diagnosed with the various forms of inherited neuropathies in order to advance therapy development for these debilitating disorders. To join the patient registry, visit www.neuropathyreg.org For further information, visit www.hnf-cure.org.


News Articles [647 Associated News Articles listed on BioPortfolio]

Santhera licences Leber’s hereditary optic neuropathy drug to Chiesi

Santhera Pharmaceuticals has licensed a drug called Raxone, indicated for the treatment of Leber’s hereditary optic neuropathy (LHON), to Chiesi...Read More... The post Santhera licences Leber’s h...

Santhera licenses Leber’s hereditary optic neuropathy drug to Chiesi

Santhera Pharmaceuticals has licensed a drug called Raxone, indicated for the treatment of Leber’s hereditary optic neuropathy (LHON), to Chiesi...Read More... The post Santhera licenses Leber’s h...

GenSight's GS010 misses in second Phase III for Leber hereditary optic neuropathy

GenSight's gene therapy GS010 fails second late-stage Leber hereditary optic neuropathy study https://www.firstwordpharma.com/node/1622917 

GenSight's gene therapy GS010 fails second late-stage Leber hereditary optic neuropathy study https://www.firstwordpharma.com/node/1622917 

Vasculitic Neuropathy: Improving Diagnostic Accuracy

SYNOPSIS: Vasculitic neuropathy is characterized by stepwise progression of sensorimotor neuropathy, usually with axonal features on electrodiagnostic studies, and often the presence of antimyeloperox...

Study offers important step to identify cause of blinding disease

Leber hereditary optic neuropathy is an inherited form of vision loss that causes people to have trouble with their color vision and difficulty seeing in the center of their visual field.

Hereditary Colon Cancer: Questions & Answers

The main hereditary colon cancers are Lynch syndrome and hereditary nonpolyposis colorectal cancer: understand the risks

Lumbosacral Radiculoplexus Neuropathy: A Case Series

Patients with diabetes are particularly susceptible to this generally painful asymmetric neuropathy.

Drugs and Medications [49 Associated Drugs and Medications listed on BioPortfolio]

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Meloxicam [kaiser foundation hospitals]

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Benzonatate [kaiser foundation hospitals]

Benzonatate Capsules, USP 100 mg

Misoprostol [kaiser foundation hospitals]

Misoprostol Tablets 8204001/0613 Rx Only

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Oxygen

PubMed Articles [685 Associated PubMed Articles listed on BioPortfolio]

Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation.

Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is characterized by adult onset, a slowly progressive course and autosomal dominant inheritance. It remains unclear ...

What are the characteristics and progression of visual field defects in patients with Leber hereditary optic neuropathy: a prospective single-centre study in China.

To study the characteristics and progression of visual field defects in patients with Leber hereditary optic neuropathy.

Functional changes of retinal ganglion cells and visual pathways in patients with Leber's hereditary optic neuropathy during one year of follow-up in chronic phase.

To assess changes of retinal ganglion cells (RGCs) and visual pathways' function in patients with Leber's hereditary optic neuropathy (LHON) during 12 months of follow-up of chronic phase.

Hereditary sensory and autonomic neuropathy type IC (HSAN1C) accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasias.

Hereditary sensory and autonomic neuropathy type I (HSAN-1) is an autosomal dominant sensory neuropathy occurring secondary to mutations in the SPTLC1 and SPTLC2 genes. We present two generations of a...

CNS Correlates of "Objective" Neuropathy in Alcohol Use Disorder.

Among the neurological consequences of alcoholism is peripheral neuropathy. Relative to HIV or diabetes-related neuropathies, neuropathy associated with Alcohol Use Disorders (AUD) is understudied. In...

Clinical Trials [1330 Associated Clinical Trials listed on BioPortfolio]

Safety and Efficacy Study of Gene Therapy for The Treatment of Leber's Hereditary Optic Neuropathy

This study is meant to evaluate the safety and efficacy of rAAV2-ND4 treatment for Leber hereditary optic neuropathy with the G11778A mutation in mitochondrial DNA.

EAP_GS010_single Patient

Expanded Access Use for a single patient of Bilateral Intravitreal Injection of GS010 in a Single Subject Affected with G11778A ND4 Leber Hereditary Optic Neuropathy

Safety and Efficacy Study of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy (LHON)

This study is meant to assess the safety and efficacy of rAAV2-ND4 treatment of Leber hereditary optic neuropathy with 11778 LHON mutation.

Historical Case Record Survey of Visual Acuity Data From Patients With Leber's Hereditary Optic Neuropathy (LHON)

The purpose of this survey is to collect visual acuity data from patients with LHON in order to establish the clinical course (natural history) and visual acuity outcomes in patients with ...

Proprioception and Sensorimotor Control in Hereditary Sensory and Atunomic Neuropathy

This project comprises three sets of physiological studies - testing eight specific hypotheses - that will contribute new knowledge on proprioception and motor control in a genetic disorde...

Companies [1478 Associated Companies listed on BioPortfolio]

Hereditary Neuropathy Foundation

Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization whose mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth disease (CMT) and ...

Neuropathy Action Foundation

Relief Therapeutics

Peripheral neuropathies are a group of conditions characterized by degeneration of peripheral motor, sensory, or autonomic nerves. Degeneration of peripheral nerves causes a wide ...

GenSight Biologics S.A.

GenSight Biologics S.A. (GenSight) is a clinical-stage biotechnology company discovering and developing novel therapies for mitochondrial and neurodegenerative diseases of the eye...

The Neuropathy Association

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