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

Year Number of Results
1984 1
1995 2
1996 1
1999 4
2006 1
2008 1
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2013 2
2014 2
2019 1
2020 1
2021 3
2024 0

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18 results

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Page 1
Peutz-Jeghers syndrome in a neonate.
Fernandez Seara MJ, Martinez Soto MI, Fernandez Lorenzo JR, Trabazo S, Gamborino E, Forteza Vila J. Fernandez Seara MJ, et al. J Pediatr. 1995 Jun;126(6):965-7. doi: 10.1016/s0022-3476(95)70224-5. J Pediatr. 1995. PMID: 7776109
Corrigendum: Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseous Heteroplasia.
Justicia-Grande AJ, Gómez-Ríal J, Rivero-Calle I, Pischedda S, Curras-Tuala MJ, Gómez-Carballa A, Cebey-López M, Pardo-Seco J, Méndez-Gallart R, Fernández-Seara MJ, Salas A, Martinón-Torres F. Justicia-Grande AJ, et al. Among authors: fernandez seara mj. Front Pediatr. 2021 Dec 14;9:807812. doi: 10.3389/fped.2021.807812. eCollection 2021. Front Pediatr. 2021. PMID: 34970520 Free PMC article.
Variations in Neonatal Length of Stay of Babies Born Extremely Preterm: An International Comparison Between iNeo Networks.
Seaton SE, Draper ES, Adams M, Kusuda S, Håkansson S, Helenius K, Reichman B, Lehtonen L, Bassler D, Lee SK, Vento M, Darlow BA, Rusconi F, Beltempo M, Isayama T, Lui K, Norman M, Yang J, Shah PS, Modi N; UK Neonatal Collaborative; International Network for Evaluating Outcomes of Neonates (iNeo) Investigators; ANZNN (Australian and New Zealand Neonatal Network); CNN (Canadian Neonatal Network); NRNJ (Neonatal Research Network Japan); SEN1500 (Spanish Neonatal Network); SwissNeoNet (Swiss Neonatal Network). Seaton SE, et al. J Pediatr. 2021 Jun;233:26-32.e6. doi: 10.1016/j.jpeds.2021.02.015. Epub 2021 Feb 15. J Pediatr. 2021. PMID: 33600820
Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseus Heteroplasia.
Justicia-Grande AJ, Gómez-Ríal J, Rivero-Calle I, Pischedda S, Curras-Tuala MJ, Gómez-Carballa A, Cebey-López M, Pardo-Seco J, Méndez-Gallart R, Fernández-Seara MJ, Salas A, Martinón-Torres F. Justicia-Grande AJ, et al. Among authors: fernandez seara mj. Front Pediatr. 2021 Jun 23;9:662669. doi: 10.3389/fped.2021.662669. eCollection 2021. Front Pediatr. 2021. PMID: 34249809 Free PMC article.
Neonatal Outcomes in Very Preterm Infants With Severe Congenital Heart Defects: An International Cohort Study.
Norman M, Håkansson S, Kusuda S, Vento M, Lehtonen L, Reichman B, Darlow BA, Adams M, Bassler D, Isayama T, Rusconi F, Lee S, Lui K, Yang J, Shah PS; International Network for Evaluation of Outcomes in Neonates (iNeo) Investigators* †. Norman M, et al. J Am Heart Assoc. 2020 Mar 3;9(5):e015369. doi: 10.1161/JAHA.119.015369. Epub 2020 Feb 21. J Am Heart Assoc. 2020. PMID: 32079479 Free PMC article.
[Partial trisomy of chromosome 5p].
Marcos Alonso S, Carreira Sande N, Couce Pico ML, Fernández Seara MJ, Fernández Bouzas R, Martínez Yriarte JM. Marcos Alonso S, et al. Among authors: fernandez seara mj. An Pediatr (Barc). 2006 Feb;64(2):185-6. doi: 10.1157/13084190. An Pediatr (Barc). 2006. PMID: 16527083 Free article. Spanish. No abstract available.
Preventive strategies and factors associated with surgically treated necrotising enterocolitis in extremely preterm infants: an international unit survey linked with retrospective cohort data analysis.
Adams M, Bassler D, Darlow BA, Lui K, Reichman B, Hakansson S, Norman M, Lee SK, Helenius KK, Lehtonen L, San Feliciano L, Vento M, Moroni M, Beltempo M, Yang J, Shah PS; International Network for EvaluatingOutcomes (iNeo) of Neonates. Adams M, et al. BMJ Open. 2019 Oct 14;9(10):e031086. doi: 10.1136/bmjopen-2019-031086. BMJ Open. 2019. PMID: 31615799 Free PMC article.
[Congenital chloridorrhea: adjuvant therapy with ibuprofen and ranitidine].
Martinón-Torres F, Fernández Seara MJ, del Río Pastoriza I, Rodrigo Sáez E, Martinón Sánchez JM, Castro-Gago M. Martinón-Torres F, et al. Among authors: fernandez seara mj. An Esp Pediatr. 1999 Jun;50(6):619-22. An Esp Pediatr. 1999. PMID: 10410429 Review. Spanish. No abstract available.
[Oculocutaneous albinism 1B associated with a new mutation in the TYR gene].
Vidal-Ríos P, Fernández-Seara MJ, Cortés E, Hurtado L, Couce ML. Vidal-Ríos P, et al. Among authors: fernandez seara mj. An Pediatr (Barc). 2013 May;78(5):339-40. doi: 10.1016/j.anpedi.2012.09.006. Epub 2012 Oct 22. An Pediatr (Barc). 2013. PMID: 23085315 Free article. Spanish. No abstract available.
18 results