Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2051-5960

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis ; volume:2 ; number:1 ; day:16 ; month:9 ; year:2014 ; pages:1-9 ; date:12.2014
Acta Neuropathologica Communications ; 2, Heft 1 (16.9.2014), 1-9, 12.2014

Creator: Hiniker, Annie

Contributor: Wong, Lee-Jun
Berven, Sigurd
Truong, Cavatina K.
Adesina, Adekunle M.
Margeta, Marta
SpringerLink (Online service)

DOI: 10.1186/s40478-014-0137-3

URN: urn:nbn:de:1111-201605067391

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Hiniker, Annie
Wong, Lee-Jun
Berven, Sigurd
Truong, Cavatina K.
Adesina, Adekunle M.
Margeta, Marta
SpringerLink (Online service)

Other Objects (12)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Infantile idiopathic scoliosis: surgical treatment in rapidly progressive cases

Adolescent idiopathic scoliosis without limb weakness: a differential diagnosis of core myopathy?

HNRNPA1 de novo variant associated with early childhood onset, rapidly progressive generalized myopathy

Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report

Rapidly increasing incidence in scoliosis surgery over 14 years in a nationwide sample

Camptocormia due to myotinilopathy, Parkinson’s disease, or both? : Camptocormia and axial myopathy

Zidovudine-induced myopathy

Centronuclear (myotubular) myopathy

Myofibrillar Myopathy Mimicking Polyneuropathy

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Related objects

Reset password