Normal view MARC view ISBD view

Young-onset parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome. [electronic resource]

By:

Mak, Chloe Miu

Contributor(s):

Producer: 20120105Description: 224-7 p. digitalISSN:

1563-5279

Subject(s):

Online resources:

Available from publisher's website

In: The International journal of neuroscience vol. 121

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Case Reports; Journal Article

There are no comments on this title.

to post a comment.

Previous

Back to results

Next

1
2
3
4
5
6
7
8
9
10
11

1 Deconstructing the molecular mechanisms of cell cycle control in a mouse adrenocortical cell line: roles of ACTH.
by Rocha, Kátia M
2 Molecular mechanisms of cell cycle control in the mouse Y1 adrenal cell line.
by Costa, Erico T
3 c-Ki-ras oncogene amplification and FGF2 signaling pathways in the mouse Y1 adrenocortical cell line.
by Forti, Fábio L
4 c-Myc protein is stabilized by fibroblast growth factor 2 and destabilized by ACTH to control cell cycle in mouse Y1 adrenocortical cells.
by Lepique, Ana Paula
5 Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.
by Yeh, Erika
6 Fibroblast growth factor 2 restrains Ras-driven proliferation of malignant cells by triggering RhoA-mediated senescence.
by Costa, Erico T
7 Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done?
by Jehee, Fernanda Sarquis
8 IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population.
by Brito, Luciano A
9 Genetic contribution for non-syndromic cleft lip with or without cleft palate (NS CL/P) in different regions of Brazil and implications for association studies.
by Brito, Luciano A
10 Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.
by Moreira, Danielle P
11 Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.
by Acuna-Hidalgo, Rocio

Close