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About 110 results

ALLMedicine™ Kennedy Disease Center

Research & Reviews  55 results

Monozygotic Twins Discordant for Kennedy Disease: A Case Report.
https://doi.org/10.1097/CND.0000000000000266
Journal of Clinical Neuromuscular Disease; Popescu C

Nov 19th, 2019 - Spinal and bulbar muscular atrophy or Kennedy disease (KD) is an X-linked recessive disorder caused by a pathogenic CAG expansion in the first exon of the androgen receptor. Proximal muscle atrophy, weakness, contraction fasciculations, bulbar inv...

MRI in Patients With Kennedy Disease
https://clinicaltrials.gov/ct2/show/NCT02501395

Jun 3rd, 2018 - Kennedy disease is an inherited neuromuscular disorder that is characterized by progressive muscle wasting and weakness. It typically starts with muscle spasms and tremors in the arms, followed by muscle weakness and atrophy of muscles in the arms...

A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.
https://doi.org/10.1002/mus.25952
Muscle & Nerve; Madeira JLO, Souza ABC et. al.

Sep 6th, 2017 - A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.|2017|Madeira JLO,Souza ABC,Cunha FS,Batista RL,Gomes NL,|genetics,physiopathology,genetics,metabolism,genetics,genetics,

Kennedy disease with difficulty in differential diagnosis: A case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428589
Medicine Chen Y, Luo P et. al.

May 10th, 2017 - Kennedy disease (KD) is also known as spinal bulbar muscular dystrophy. As KD has similar symptoms with most neuromuscular diseases, so it is difficult to make a rapid diagnosis clinically. We report a case of a 43-year-old male with progressive l...

Spinal and Bulbar Muscular Atrophy.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628725
Neurologic Clinics; Grunseich C, Fischbeck KH

Oct 30th, 2015 - Spinal and bulbar muscular atrophy, or Kennedy disease, is a slowly progressive X-linked neuromuscular disease caused by a trinucleotide (CAG) repeat expansion in the androgen receptor gene. Affected males typically develop weakness in their mid-4...

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Clinicaltrials.gov  55 results

Monozygotic Twins Discordant for Kennedy Disease: A Case Report.
https://doi.org/10.1097/CND.0000000000000266
Journal of Clinical Neuromuscular Disease; Popescu C

Nov 19th, 2019 - Spinal and bulbar muscular atrophy or Kennedy disease (KD) is an X-linked recessive disorder caused by a pathogenic CAG expansion in the first exon of the androgen receptor. Proximal muscle atrophy, weakness, contraction fasciculations, bulbar inv...

MRI in Patients With Kennedy Disease
https://clinicaltrials.gov/ct2/show/NCT02501395

Jun 3rd, 2018 - Kennedy disease is an inherited neuromuscular disorder that is characterized by progressive muscle wasting and weakness. It typically starts with muscle spasms and tremors in the arms, followed by muscle weakness and atrophy of muscles in the arms...

A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.
https://doi.org/10.1002/mus.25952
Muscle & Nerve; Madeira JLO, Souza ABC et. al.

Sep 6th, 2017 - A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.|2017|Madeira JLO,Souza ABC,Cunha FS,Batista RL,Gomes NL,|genetics,physiopathology,genetics,metabolism,genetics,genetics,

Kennedy disease with difficulty in differential diagnosis: A case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428589
Medicine Chen Y, Luo P et. al.

May 10th, 2017 - Kennedy disease (KD) is also known as spinal bulbar muscular dystrophy. As KD has similar symptoms with most neuromuscular diseases, so it is difficult to make a rapid diagnosis clinically. We report a case of a 43-year-old male with progressive l...

Spinal and Bulbar Muscular Atrophy.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628725
Neurologic Clinics; Grunseich C, Fischbeck KH

Oct 30th, 2015 - Spinal and bulbar muscular atrophy, or Kennedy disease, is a slowly progressive X-linked neuromuscular disease caused by a trinucleotide (CAG) repeat expansion in the androgen receptor gene. Affected males typically develop weakness in their mid-4...

see more →