Alpha-fetoprotein, a fascinating protein and biomarker in neurology.

[1]  D. Piccini,et al.  Senataxin Associates with Replication Forks to Protect Fork Integrity across RNA-Polymerase-II-Transcribed Genes , 2012, Cell.

[2]  S. Seneca,et al.  Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy. , 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[3]  M. D. Del Bigio,et al.  Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia , 2012, Case reports in pediatrics.

[4]  N. Patni,et al.  Elevated α-fetoprotein levels in Van Wyk-Grumbach syndrome: a case report and review of literature , 2012 .

[5]  A. Broeks,et al.  Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia‐telangiectasia: A genotype–phenotype study , 2012, Human mutation.

[6]  M. Koenig,et al.  The autosomal recessive cerebellar ataxias. , 2012, The New England journal of medicine.

[7]  P. Bavi,et al.  A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia , 2012, Human mutation.

[8]  M. Blankenstein,et al.  Performance of first‐trimester combined test for Down syndrome in different maternal age groups: reason for adjustments in screening policy? , 2011, Prenatal diagnosis.

[9]  B. Kremer,et al.  Autosomal recessive cerebellar ataxias: the current state of affairs , 2011, Journal of Medical Genetics.

[10]  J. Pedroso,et al.  Alpha-fetoprotein as a biomarker for recessive ataxias. , 2010, Arquivos de neuro-psiquiatria.

[11]  J. Giltay,et al.  Hereditary persistence of alpha-fetoprotein (HPAF P): review of the literature. , 2010, The Netherlands journal of medicine.

[12]  A. Seller,et al.  The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO , 2010, Neurology.

[13]  N. Drouot,et al.  Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. , 2009, Brain : a journal of neurology.

[14]  W. F. Abdo,et al.  Clinical spectrum of ataxia-telangiectasia in adulthood , 2009, Neurology.

[15]  M. Koenig,et al.  Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients , 2009, Journal of the Neurological Sciences.

[16]  S. Hirohashi,et al.  Molecular background of α‐fetoprotein in liver cancer cells as revealed by global RNA expression analysis , 2008, Cancer science.

[17]  J. Loeber,et al.  Fifteen years of triple tests in The Netherlands; the life cycle of a screening test , 2008, Prenatal diagnosis.

[18]  Joris R Delanghe,et al.  Diagnosing and monitoring hepatocellular carcinoma with alpha-fetoprotein: new aspects and applications. , 2008, Clinica chimica acta; international journal of clinical chemistry.

[19]  A. Børresen-Dale,et al.  Alpha fetoprotein is increasing with age in ataxia-telangiectasia. , 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[20]  G. Mizejewski.  Physiology of Alpha-Fetoprotein as a Biomarker for Perinatal Distress: Relevance to Adverse Pregnancy Outcome , 2007, Experimental biology and medicine.

[21]  K. Dalhoff,et al.  Alpha‐fetoprotein is a predictor of outcome in acetaminophen‐induced liver injury , 2005, Hepatology.

[22]  A. Riskin,et al.  Alpha-fetoprotein in the early neonatal period--a large study and review of the literature. , 2004, Clinica chimica acta; international journal of clinical chemistry.

[23]  C. Broeckhoven,et al.  POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement , 2004, Neurology.

[24]  R. Sharony,et al.  Congenital deficiency of alpha feto-protein , 2004, European Journal of Human Genetics.

[25]  Y. Agid,et al.  Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients. , 2004, Brain : a journal of neurology.

[26]  S. Rivaud-Pechoux,et al.  Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies. , 2003, Brain : a journal of neurology.

[27]  G. Mizejewski.  Levels of Alpha-Fetoprotein During Pregnancy and Early Infancy in Normal and Disease States , 2003, Obstetrical & gynecological survey.

[28]  J. Nichols,et al.  Alpha-fetoprotein, the major fetal serum protein, is not essential for embryonic development but is required for female fertility , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[29]  R. Shawky,et al.  Alphafetoprotein in screening for congenital hypothyroidism. , 2001, Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit.

[30]  G. Mizejewski,et al.  Alpha-fetoprotein Structure and Function: Relevance to Isoforms, Epitopes, and Conformational Variants , 2001, Experimental biology and medicine.

[31]  U. Göbel,et al.  Alpha1-Fetoprotein (AFP) Reference Values in Infants up to 2 Years of Age , 1998 .

[32]  J. Ingrand,et al.  [Alpha fetoprotein in congenital hypothyroidism before and during treatment]. , 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[33]  S. Yagel,et al.  Physiology: The regulatory role of tri-iodothyronine on the production of α-fetoprotein and albumin by mouse fetal liver cells , 1993 .

[34]  R. Krumlauf,et al.  A G → A substitution in an HNF I binding site in the human α-fetoprotein gene is associated with hereditary persistence of α-fetoprotein (HPAFP) , 1993 .

[35]  E. Rose,et al.  Alpha-fetoprotein levels in normal adults. , 1992, The American journal of the medical sciences.

[36]  K. Taketa,et al.  Tissue of origin of elevated alpha-fetoprotein in ataxia-telangiectasia. , 1986, Disease markers.

[37]  W. Mortensson,et al.  SERUM α‐FETOPROTEIN—A BIOCHEMICAL INDICATOR OF PRENATAL HYPOTHYROIDISM , 1983 .

[38]  T. Waldmann,et al.  Serum-alpha-fetoprotein levels in patients with ataxia-telangiectasia. , 1972, Lancet.

[39]  E. Milgrom,et al.  Hereditary persistence of α-fetoprotein is due to both proximal and distal hepatocyte nuclear factor-1 site mutations1 , 2004 .

[40]  N. Lazarevich.  Molecular mechanisms of alpha-fetoprotein gene expression. , 2000, Biochemistry. Biokhimiia.

[41]  S. Pantelakis,et al.  α-Fetoprotein in Congenital Hypothyroidism , 1990 .

[42]  C G BERGSTRAND,et al.  Demonstration of a new protein fraction in serum from the human fetus. , 1956, Scandinavian journal of clinical and laboratory investigation.