Mutation in the Methylenetetrahydrofolate Reductase Gene Might Be a Risk Factor for Cerebrovascular Disease in Peripartum and Under Oral Contraceptive Use

By  

European Neurology, Vol. 45, Iss. 3, 2001-04 ,pp. : 171-173

Karger

Access to resources Recommend Favorite

A Novel Type of Mutation at the Propeptide Cleavage Site (AlA+1Thr) Causing Symptomatic Protein C Type II Deficiency

By Dodojacek R.   Hofler G.   Leschnik B.   Muntean W.  

Thrombosis Research, Vol. 100, Iss. 1, 2000-10 ,pp. : 109-113

Elsevier

Access to resources Recommend Favorite

MYH9 related disease: A novel missense Ala95Asp mutation of the MYH9 gene

By de Rocco Daniela   Heller Paula G.   Girotto Giorgia   Pastore Annalisa   Glembotsky Ana C.   Marta Rosana F.   Bozzi Valeria   Pecci Alessandro   Molinas Felisa C.   Savoia Anna  

Platelets, Vol. 20, Iss. 8, 2009-08 ,pp. : 598-602

Informa Healthcare

Access to resources Recommend Favorite

Plasma Lipoprotein(a) Levels Are High in Patients with Central Retinal Artery Occlusion - Detection of an Ala601-Thr Mutation in 118 out of 125 families and identification of a new Asp676-Asn mutation

By Murata M.   Saito T.   Takahashi S.   Ichinose A.  

Thrombosis Research, Vol. 91, Iss. 4, 1998-08 ,pp. : 169-175

Elsevier

Access to resources Recommend Favorite

No Mutation of G209A in the Alpha-Synuclein Gene in Sporadic Parkinson’s Disease among Taiwan Chinese

By  

European Neurology, Vol. 41, Iss. 2, 1999-02 ,pp. : 85-87

Karger

Access to resources Recommend Favorite