News Article Archive : Resources : Spastic Paraplegia Foundation

February 5, 2025

Spinal stimulation restored muscles wasted by rare genetic disorder

byJon Hamilton, Rhode Island PBS

January 23, 2025

The Top Stories That Defined Exoskeleton Technology in 2024

byThe Exoskeleton Report 1/6/25

December 27, 2024

Restoring adapter protein complex 4 function with small molecules: an in silico approach to spastic paraplegia 50

October 18, 2024

Axon-specific microtubule regulation drives asymmetric regeneration 2 of sensory neuron axons

byAna C. Costa, Blanca R. Murillo, Rita Bessa, Ricardo Ribeiro, Tiago Ferreira da Silva, Patrícia Porfírio-Rodrigues , Gabriel G. Martins , Pedro Brites , Matthias Kneussel, Thomas Misgeld, Monika S. Brill , Monica M. Sousa

September 13, 2024

YouTube Video: What is Hereditary Spastic Paraplegia

byPatrick Malone

September 10, 2024

Dayna (with HSP) defeats demons to claim Bronze in Paris

byMarcus Uhe, Berwick Star News

September 5, 2024

Pittsburgh Native , Rebecca Hart (with HSP). Wins Gold Medal In 2024 Paralympics

byEric Heyl, Pittsburg News

August 22, 2024

Preclinical alternative drug discovery programs for monogenic rare diseases. The case of hereditary spastic paraplegias

byMatteo Rossi Sebastiano, Shinji Hadano, Fabrizia Cesca, Giuseppe Ermondi

August 17, 2024

Create Your Legal Fee Will and Legacy! August is National Make-A-Will Month!

byFreeWill

July 3, 2024

A Wheelchair User’s Guide to Shoulder Treatments

byBob Vogel, New Mobility Magazine

July 1, 2024

The Journey of CRISPR-Cas9, The past, present, and future of gene editing

byJon Chesnut, The Medicine Maker

July 1, 2024

Researchers Publish 'Revolutionary' Gene Editing Findings

bySean Ashcroft, Healthcare Digital

June 30, 2024

Neurodegeneration Due to Ultra-Rare Disease (SPG50 HSP) Slowed by AAV Gene Therapy

byGenetic Engineering and Biotechnology News

June 27, 2024

Download recent PhD Dissertation: MECHANISMS LINKING MITOCHONDRIAL DYNAMICS, MICROTUBULE MOTORS, AND NEUROLOGICAL DISEASE

byAdam Ray Fenton, University of Pennsylvania

June 21, 2024

MorphGrower: A Synchronized Layer-by-layer Growing Approach for Plausible Neuronal Morphology Generation

byNianzu Yang Kaipeng Zeng Haotian Lu Yexin Wu Zexin Yuan Dan

June 17, 2024

Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons

byEliska Zlamalova, Catherine Rodger, Francesca Greco, Samuel R. Cheers, Julia Kleniuk, Aishwarya G. Nadadhur, Zuzana Kadlecova, Evan Reid

June 17, 2024

Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia

byAlzhraa A Ibrahim, Malte Ollenschläger, Stephan Klebe, Rebecca Schüle, Nicole Jeschonneck, Melanie Kellner, Evelyn Loris, Teresa Greinwalder, Bjoern M Eskofier, Jürgen Winkler, Heiko Gaßner, Martin Regensburger

June 17, 2024

Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice

byManon Fortier, Margaux Cauhapé, Suzie Buono, Julien Becker, Alexia Menuet, Julien Branchu, Ivana Ricca, Serena Mero, Karim Dorgham, Khalid-Hamid El Hachimi, Kostantin Dobrenis, Benoit Colsch, Dominic Samaroo, Morgan Devaux, Ale

June 11, 2024

Recap Wearable Technologies Conference EU 2024

byWearable Technologies Online Magazine

June 11, 2024

Medicare Sets Reimbursement Rates for Personal Exoskeletons: A Milestone for Accessibility

byExoskeleton Report

April 26, 2024

The journey to a treatment for hereditary spastic paraplegia

byNancy Fliesler, Boston Children's Hospital

April 15, 2024

Columbia gets $15M to design gene therapies for rare ALS forms

byALS News Today

April 15, 2024

The Best Small Town in Each State

byBradley O'Neil, The Discover

April 12, 2024

Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing

byYue-Ting Deng, Bang-Sheng Wu, Liu Yang, Xiao-Yu He, Ju-Jiao Kang, Wei-Shi Liu, Ze-Yu Li, Xin-Rui Wu, Ya-Ru Zhang, Shi-Dong Chen, Yi-Jun Ge, Yu-Yuan Huang, Jian-Feng Feng, Ying Zhu, Qiang Dong, Ying Mao, Wei Cheng & Jin-Tai Yu

April 12, 2024

Gangliosides as Therapeutic Targets for Neurodegenerative Diseases

byOrhan Kerim Inci, Hande Basırlı, Melike Can, Selman Yanbul, and Volkan Seyrantepe

News Article Archive

News Articles

Spinal stimulation restored muscles wasted by rare genetic disorder

The Top Stories That Defined Exoskeleton Technology in 2024

Restoring adapter protein complex 4 function with small molecules: an in silico approach to spastic paraplegia 50

Axon-specific microtubule regulation drives asymmetric regeneration 2 of sensory neuron axons

YouTube Video: What is Hereditary Spastic Paraplegia

Dayna (with HSP) defeats demons to claim Bronze in Paris

Pittsburgh Native , Rebecca Hart (with HSP). Wins Gold Medal In 2024 Paralympics

Preclinical alternative drug discovery programs for monogenic rare diseases. The case of hereditary spastic paraplegias

Create Your Legal Fee Will and Legacy! August is National Make-A-Will Month!

A Wheelchair User’s Guide to Shoulder Treatments

The Journey of CRISPR-Cas9, The past, present, and future of gene editing

Researchers Publish 'Revolutionary' Gene Editing Findings

Neurodegeneration Due to Ultra-Rare Disease (SPG50 HSP) Slowed by AAV Gene Therapy

Download recent PhD Dissertation: MECHANISMS LINKING MITOCHONDRIAL DYNAMICS, MICROTUBULE MOTORS, AND NEUROLOGICAL DISEASE

MorphGrower: A Synchronized Layer-by-layer Growing Approach for Plausible Neuronal Morphology Generation

Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons

Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia

Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice

Recap Wearable Technologies Conference EU 2024

Medicare Sets Reimbursement Rates for Personal Exoskeletons: A Milestone for Accessibility

The journey to a treatment for hereditary spastic paraplegia

Columbia gets $15M to design gene therapies for rare ALS forms

The Best Small Town in Each State

Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing

Gangliosides as Therapeutic Targets for Neurodegenerative Diseases

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