Altered apoptosis regulation in kufor-rakeb syndrome patients with mutations in

Aug 23, 2011 . Kufor-Rakeb syndrome symptoms, causes, diagnosis, and treatment information

May 8, 2007 . pyramidal disease Kufor-Rakeb syndrome (KRS). KRS was originally described

Aug 26, 2011 . Mutations in the ATP13A2 gene are associated with Kufor-Rakeb syndrome (KRS) and

Aug 3, 2010 . We report the clinical features of the original Chilean family with Kufor-Rakeb

Dec 8, 2011 . BioInfoBank Library :: Altered apoptosis regulation in kufor-rakeb syndrome

Dec 5, 2011 . References. OMIM [1]. Kufor-Rakeb syndrome (Parkinson disease-9). Retrieved

Apr 15, 2008 . ism, or Kufor-Rakeb syndrome (KRS), is charac- terized by subacute or slowly

Mutations in ATP13A2 (PARK9) have been linked to juvenile parkinsonism with

5. März 2010 . Abstract. Das Kufor-Rakeb Syndrom (KRS) ist eine seltene, neurodegenerative

Kufor-Rakeb syndrome is an autosomal recessive disorder. . "Kufor Rakeb

Kufor-Rakeb syndrome is an autosomal recessive nigro-striatal-pallidal-

Kufor-Rakeb Syndrome Kufor-Rakeb syndrome is a rare autosomal recessive

NEUROGENETICS It has been suggested that pallidopyramidal disease is reces-

Recessively inherited mutations in ATP13A2 result in Kufor-Rakeb syndrome,

Altered apoptosis regulation in kufor-rakeb syndrome patients with mutations in

Kufor-Rakeb syndrome is an autosomal recessive disorder. It can be associated

KUFOR-RAKEB SYNDROME. Synonym Acr. KRS. KRPPD. PARK9. Synonym

606693 - KUFOR-RAKEB SYNDROME; KRS - PARKINSON DISEASE 9,

Feb 23, 2011 . The Kufor–Rakeb syndrome is a neurodegenerative disease, considered a form

Short report. Kufor-Rakeb syndrome, pallido-pyramidal degeneration with

(2011) Tan et al. The Journal of Biological Chemistry. Read by researchers in:

Kufor-Rakeb syndrome is an autosomal recessive disorder. . Description above

Aug 26, 2011 . Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-

We report the clinical features of the original Chilean family with Kufor-Rakeb

(2002). "Kufor-Rakeb syndrome, pallido-pyramidal degeneration with

http://www.w3.org/2000/01/rdf-schema#label, KUFOR-RAKEB SYNDROME. http://link.

On the other hand, Kufor-Rakeb syndrome has additional signs, which

Jun 23, 2011 . Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (

Detection of Protein Ubiquitination. Ubiquitination, the covalent .

2009; 47(Suppl1):S75–S81 Kufor-Rakeb disease [OMIM#606693] PARK9 .

Kufor-Rakeb syndrome. Najim Al-Din AS, Wriekat A, Mubaidin A, Dasouki M,

J Med Genet. 2001 Oct;38(10):680-2. Kufor-Rakeb syndrome, pallido-pyramidal

Aug 26, 2011 . Mutations in the ATP13A2 gene are associated with Kufor-Rakeb syndrome (

How "KUFOR RAKEB SYNDROME" is abbreviated or used as part of acronym or

Sep 2, 2009 . Kufor-Rakeb syndrome is an autosomal recessive nigro-striatal-pallidal-

Kufor-Rakeb syndrome is an autosomal recessive nigro-striatal-pallidal-

Aug 30, 2010 . Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2

Mutations in ATP13A2 were initially identified in patients with Kufor-Rakeb

Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia:

Tan J, The Journal of biological chemistry, Mutations in the ATP13A2 gene are

KUFOR RAKEB SYNDROME Abbreviations and Acronyms / Abbreviated As - 1 Records.

Kufor-Rakeb syndrome (parkinsonism type 9, PARK9, pallidopyramidal

pedigree with Kufor-Rakeb syndrome (KRS). Interventions: Clinical

Feb 27, 2010 . Kufor-Rakeb Syndrome. Classification and external resources. OMIM · 610513 ·

Jul 1, 2011 . Mutations in the ATP13A2 gene are associated with Kufor-Rakeb syndrome (

Kufor-Rakeb syndrome is a juvenile-onset neurodegenerative disorder with an

Parkinson disease (autosomal recessive) 9 (Kufor-Rakeb syndrome), EC 3.6.3 .

Jul 18, 2011 . Kufor-Rakeb syndrome (KRS) is a rare autosomal recessive inherited juvenile

Sep 15, 2010 . We report the clinical features of the original Chilean family with Kufor-Rakeb

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