Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2377

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism ; volume:11 ; number:1 ; day:17 ; month:6 ; year:2011 ; pages:1-3 ; date:12.2011
BMC neurology ; 11, Heft 1 (17.6.2011), 1-3, 12.2011

Creator: Serikawa, Takehiro

Contributor: Shimohata, Takayoshi
Akashi, Mami
Yokoseki, Akio
Tsuchiya, Miwa
Hasegawa, Arika
Haino, Kazufumi
Koike, Ryoko
Takakuwa, Koichi
Tanaka, Keiko
Tanaka, Kenichi
Nishizawa, Masatoyo
SpringerLink (Online service)

DOI: 10.1186/1471-2377-11-72

URN: urn:nbn:de:1111-2016030328947

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 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

Serikawa, Takehiro
Shimohata, Takayoshi
Akashi, Mami
Yokoseki, Akio
Tsuchiya, Miwa
Hasegawa, Arika
Haino, Kazufumi
Koike, Ryoko
Takakuwa, Koichi
Tanaka, Keiko
Tanaka, Kenichi
Nishizawa, Masatoyo
SpringerLink (Online service)

Other Objects (12)

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Hochschulschrift

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Hochschulschrift

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Hochschulschrift

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

Hochschulschrift

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Hochschulschrift

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Hochschulschrift

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Hochschulschrift

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

Hochschulschrift

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Hochschulschrift

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Hochschulschrift

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Hochschulschrift

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

Hochschulschrift

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

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.

Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

Autosomal recessive cerebellar ataxias

Genetics of autosomal recessive intellectual disability

Autosomal recessive myotonia congenita in sheep

Molecular characterisation of Parkin-associated parkinsonism in a human cellular model

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

Milestone discoveries of autosomal recessive childhood proximal spinal muscular atrophies

Investigation of the genetical basis of autosomal recessive Cutis Laxa

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy

The role of CDK5RAP2 in autosomal recessive primary microcephaly (MCPH)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

Related objects

Reset password