Castro Barbero, Maria Luisa marialuisa.castro@uam.es

Publications

PAH deficient pathology in humanized c.1066-11G>A phenylketonuria mice

  • Martínez-Pizarro, A
  • Picó, S
  • López-Márquez, A
  • Rodriguez-López, C
  • Montalvo, E
  • Alvarez, M
  • Castro, M
  • Ramón-Maiques, S
  • Pérez, B
  • Lucas, JJ
  • Richard, E
  • Desviat, LR
... View more Collapse

Human Molecular Genetics (p. 1074-1089) - 5/6/2024

10.1093/hmg/ddae051 View at source

  • ISSN 14602083

Splice-Switching Antisense Oligonucleotides Correct Phenylalanine Hydroxylase Exon 11 Skipping Defects and Rescue Enzyme Activity in Phenylketonuria

  • Martinez-Pizarro, A
  • Alvarez, M
  • Dembic, M
  • Lindegaard, CA
  • Castro, M
  • Richard, E
  • Andresen, BS
  • Desviat, LR
... View more Collapse

Nucleic Acid Therapeutics (p. 134-142) - 1/1/2024

10.1089/nat.2024.0014 View at source

  • ISSN 21593337

CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington’s disease

  • Picó, S
  • Parras, A
  • Santos-Galindo, M
  • Pose-Utrilla, J
  • Castro, M
  • Fraga, E
  • Hernández, IH
  • Elorza, A
  • Anta, H
  • Wang, N
  • Martí-Sánchez, L
  • Belloc, E
  • Garcia-Esparcia, P
  • Garrido, JJ
  • Ferrer, I
  • Macías-García, D
  • Mir, P
  • Artuch, R
  • Pérez, B
  • Hernández, F
  • Navarro, P
  • López-Sendón, JL
  • Iglesias, T
  • Yang, XW
  • Méndez, R
  • Lucas, JJ
... View more Collapse

Science Translational Medicine - 29/9/2021

10.1126/scitranslmed.abe7104 View at source

  • ISSN 19466234

Arteterapia en dolor crónico

  • Bermúdez Castro, Marge Andrea
  • del Río Diéguez, María
  • Palao Tarrero, Angela

Metas De Enfermería (p. 28-32) - 1/1/2019

10.35667/metasenf.2019.22.1003081410 View at source

  • ISSN 11387262

Niños de altas capacidades intelectuales: ¿niños en riesgo social?

  • Castro Barbero, María Luisa

Educación Y Futuro. Revista De Investigación Aplicada Y Experiencias Educativas (p. 163-176) - 1/1/2008

  • ISSN 15765199
  • iMarina

Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR geness: Is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?

  • Martinez-Frias, ML
  • Perez, B
  • Desviat, LR
  • Castro, M
  • Leal, F
  • Rodriguez, L
  • Mansilla, E
  • Martinez-Fernandez, ML
  • Bermejo, E
  • Rodriguez-Pinilla, E
  • Prieto, D
  • Ugarte, M
... View more Collapse

American Journal Of Medical Genetics Part a (p. 987-997) - 1/5/2006

10.1002/ajmg.a.31203 View at source

  • ISSN 15524825

Liver transplantation in nine Spanish patients with tyrosinaemia type I

  • Perez-Cerda, C
  • Merinero, B
  • Sanz, P
  • Castro, M
  • Gangoiti, J
  • Garcia, M J
  • Diaz, M
  • Medina, E
  • Ugarte, M
... View more Collapse

Journal Of Inherited Metabolic Disease (p. 119-122) - 1/1/1995

7564224 View at source

  • ISSN 01418955

The key role of sodium in the ouabain-mediated potentiation of potassium-evoked catecholamine release in cat adrenal glands

  • Abajo F
  • Castro M
  • Sanchez-Garcia P

British Journal Of Pharmacology (p. 455-462) - 1/1/1989

10.1111/j.1476-5381.1989.tb12618.x View at source

  • ISSN 00071188

Catecholamine release evoked by lithium from the perfused adrenal gland of the cat

  • Abajo F
  • Castro M
  • Garijo B
  • Sánchez‐García P

British Journal Of Pharmacology (p. 539-546) - 1/1/1987

10.1111/j.1476-5381.1987.tb11247.x View at source

  • ISSN 00071188

Conocimientos y actitudes de maestros de Educación Infantil, Educación Primaria y estudiantes de magisterio sobre los niños superdotados intelectualmente

  • Castro Barbero, María Luisa

(p. - ) - 1/1/2006

  • ISBN 8466927352
  • iMarina

This researcher has no book chapters.

MILD HOMOCYSTEINEMIA AND METHYLMALONIC ACIDURIA IN A CASE WITH PANCYTOPENIA DUE TO TRANSCOBALAMIN II DEFICIENCY

  • Merinero, B
  • Lama, R
  • Moráis, A
  • Sala, PR
  • Sanz, P
  • Castro, M
  • García, MJ
  • Leal, F
  • Pérez-Cerdá, C
  • Pérez, B
  • Ugarte, M
... View more Collapse

Journal Of Inherited Metabolic Disease (p. S158-S158) - 1/1/2010

  • ISSN 01418955
  • iMarina

LIVER-TRANSPLANTATION IN 9 SPANISH PATIENTS WITH TYROSINEMIA TYPE-I

  • Ugarte Perez, Magdalena
  • Perezcerda, C
  • Merinero, B
  • Sanz, P
  • Castro, M
  • Gangoiti, J
  • Garcia, MJ
  • Diaz, M
  • Medina, E
... View more Collapse

Journal Of Inherited Metabolic Disease (p. 119-122) - 1/3/1995

10.1007/bf00711744 View at source

  • ISSN 01418955

Screening for adenylosuccinate lyase deficiency: clinical, biochemical and molecular findings in four patients

  • Castro, M
  • Pérez-Cerdá, C
  • Merinero, B
  • García, MJ
  • Bernar, J
  • Nagel, AG
  • Torres, J
  • Bermúdez, M
  • Garavito, P
  • Marie, S
  • Vincent, F
  • Van den Berghe, G
  • Ugarte, M
... View more Collapse

Neuropediatrics (p. 186-189) - 1/8/2002

10.1055/s-2002-34493 View at source

  • ISSN 0174304X

Adolescent myopathic presentation in two sisters with very long-chain acyl-CoA dehydrogenase deficiency

  • Merinero, B
  • Pascual, SIP
  • Pérez-Cerdá, C
  • Gangoiti, J
  • Castro, M
  • Garcia, MJ
  • Castroviejo, IP
  • Vianey-Saban, C
  • Andresen, B
  • Gregersen, N
  • Ugarte, M
... View more Collapse

Journal Of Inherited Metabolic Disease (p. 802-810) - 1/1/1999

10.1023/a:1005553907216 View at source

  • ISSN 01418955

This researcher has no technical reports.

This researcher has no research projects.

This researcher has no supervised thesis.

This researcher has no patents or software licenses.

Last data update: 2/15/26 1:19 AM