Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 2
2014 1
2017 1
2019 3
2021 1
2022 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

9 results

Results by year

Filters applied: . Clear all
Page 1
Aproximación etiológica a la hipoglucemia en urgencias: revisión de un protocolo.
Pérez Delgado R, Soria Marzo A, García Jiménez I, Campos Calleja C, García Mata JR, Lafuente Hidalgo M, García Oguiza A, López Pisón J, Luis Peña Segura J, Baldellou Vázquez A. Pérez Delgado R, et al. Among authors: garcia jimenez i. Rev Calid Asist. 2008 Jul;23(4):194-6. doi: 10.1016/S1134-282X(08)72133-X. Epub 2008 Oct 26. Rev Calid Asist. 2008. PMID: 23040192 Spanish. No abstract available.
Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders.
Alfonsi C, Stephan-Otto C, Cortès-Saladelafont E, Palacios NJ, Podzamczer-Valls I, Cruz NG, Jiménez MRD, Micó SI, Vila MT, Jeltsch K, Hübschmann OK, Opladen T, Fragua RV, Gómez T, Fortuny OA, Jiménez IG, Laso EL, Martínez AR, López JM, Garcia-Cazorla À. Alfonsi C, et al. Among authors: jimenez ig. Neuroradiology. 2022 Nov;64(11):2179-2190. doi: 10.1007/s00234-022-02989-8. Epub 2022 Jun 4. Neuroradiology. 2022. PMID: 35662359
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain.
Medrano C, Vega A, Navarrete R, Ecay MJ, Calvo R, Pascual SI, Ruiz-Pons M, Toledo L, García-Jiménez I, Arroyo I, Campo A, Couce ML, Domingo-Jiménez MR, García-Silva MT, González-Gutiérrez-Solana L, Hierro L, Martín-Hernández E, Martínez-Pardo M, Roldán S, Tomás M, Cabrera JC, Mártinez-Bugallo F, Martín-Viota L, Vitoria-Miñana I, Lefeber DJ, Girós ML, Serrano Gimare M, Ugarte M, Pérez B, Pérez-Cerdá C. Medrano C, et al. Among authors: garcia jimenez i. Clin Genet. 2019 May;95(5):615-626. doi: 10.1111/cge.13508. Epub 2019 Apr 3. Clin Genet. 2019. PMID: 30653653
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment.
Bravo-Alonso I, Navarrete R, Vega AI, Ruíz-Sala P, García Silva MT, Martín-Hernández E, Quijada-Fraile P, Belanger-Quintana A, Stanescu S, Bueno M, Vitoria I, Toledo L, Couce ML, García-Jiménez I, Ramos-Ruiz R, Martín MÁ, Desviat LR, Ugarte M, Pérez-Cerdá C, Merinero B, Pérez B, Rodríguez-Pombo P. Bravo-Alonso I, et al. Among authors: garcia jimenez i. J Clin Med. 2019 Nov 1;8(11):1811. doi: 10.3390/jcm8111811. J Clin Med. 2019. PMID: 31683770 Free PMC article.
[Cyanosis after topical anesthesia administration].
Bancalero Flores JL, Bocos Terraz P, García Jiménez I, Pérez Lungmus G. Bancalero Flores JL, et al. Among authors: garcia jimenez i. Med Clin (Barc). 2008 Jun 7;131(1):35-6. doi: 10.1157/13123039. Med Clin (Barc). 2008. PMID: 18582423 Spanish. No abstract available.
[Calcifications in cranial CT scan, hypopigmented macula… What is it?].
Rubio Sánchez P, García Jiménez I, López Pisón J. Rubio Sánchez P, et al. Among authors: garcia jimenez i. An Pediatr (Engl Ed). 2022 Aug;97(2):143-145. doi: 10.1016/j.anpedi.2021.04.016. Epub 2021 Jun 3. An Pediatr (Engl Ed). 2022. PMID: 34092501 Free article. Spanish. No abstract available.
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program.
Navarrete R, Leal F, Vega AI, Morais-López A, Garcia-Silva MT, Martín-Hernández E, Quijada-Fraile P, Bergua A, Vives I, García-Jiménez I, Yahyaoui R, Pedrón-Giner C, Belanger-Quintana A, Stanescu S, Cañedo E, García-Campos O, Bueno-Delgado M, Delgado-Pecellín C, Vitoria I, Rausell MD, Balmaseda E, Couce ML, Desviat LR, Merinero B, Rodríguez-Pombo P, Ugarte M, Pérez-Cerdá C, Pérez B. Navarrete R, et al. Among authors: garcia jimenez i. Eur J Hum Genet. 2019 Apr;27(4):556-562. doi: 10.1038/s41431-018-0330-0. Epub 2019 Jan 9. Eur J Hum Genet. 2019. PMID: 30626930 Free PMC article.
[A regenerative anemia in infants: 2 cases of Pearson´s syndrome].
Martínez de Zabarte Fernández JM, Rodríguez-Vigil Iturrate C, Martínez Faci C, García Jiménez I, Murillo Sanjuan L, Muñoz Mellado A. Martínez de Zabarte Fernández JM, et al. Among authors: garcia jimenez i. Arch Argent Pediatr. 2017 Feb 1;115(1):e24-e27. doi: 10.5546/aap.2017.e24. Arch Argent Pediatr. 2017. PMID: 28097850 Free article. Spanish.
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases.
Martín-Hernández E, Aldámiz-Echevarría L, Castejón-Ponce E, Pedrón-Giner C, Couce ML, Serrano-Nieto J, Pintos-Morell G, Bélanger-Quintana A, Martínez-Pardo M, García-Silva MT, Quijada-Fraile P, Vitoria-Miñana I, Dalmau J, Lama-More RA, Bueno-Delgado MA, Del Toro-Riera M, García-Jiménez I, Sierra-Córcoles C, Ruiz-Pons M, Peña-Quintana LJ, Vives-Piñera I, Moráis A, Balmaseda-Serrano E, Meavilla S, Sanjurjo-Crespo P, Pérez-Cerdá C. Martín-Hernández E, et al. Among authors: garcia jimenez i. Orphanet J Rare Dis. 2014 Nov 30;9:187. doi: 10.1186/s13023-014-0187-4. Orphanet J Rare Dis. 2014. PMID: 25433810 Free PMC article.