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Items: 1 to 20 of 26

1.

Deficiencia de vitamina D en niños aragoneses sanos.

Martínez Redondo I, García Romero R, Calmarza P, De Arriba Muñoz A, Rodríguez Martínez G, Labarta Aizpún JI.

Nutr Hosp. 2018 Apr 27;35(4):782-788. doi: 10.20960/nh.1592. Spanish.

2.

[Natural progression of premature pubarche and underlying diseases].

Sancho Rodríguez ML, Bueno Lozano G, Labarta Aizpún JI, de Arriba Muñoz A.

An Pediatr (Barc). 2018 Oct;89(4):238-245. doi: 10.1016/j.anpedi.2017.11.012. Epub 2018 Apr 25. Spanish.

3.

3β-hydroxyesteroid dehydrogenase deficiency detected through increased serum levels of 17-hydroxyprogesterone in the neonatal screening.

de Arriba Muñoz A, Izquierdo Álvarez S, Labarta Aizpún JI.

Med Clin (Barc). 2018 Jan 31. pii: S0025-7753(17)30963-6. doi: 10.1016/j.medcli.2017.12.004. [Epub ahead of print] English, Spanish. No abstract available.

PMID:
29397097
4.

Mayer-Rokitansky-Küster-Hauser syndrome: two case reports.

Sánchez Malo MJ, Arrudi Moreno M, de Arriba Muñoz A.

Med Clin (Barc). 2018 Jul 23;151(2):e9-e10. doi: 10.1016/j.medcli.2017.11.034. Epub 2017 Dec 29. English, Spanish. No abstract available.

PMID:
29292105
5.

Hypoparathyroidism and disorder of sex development: A rare association.

Vera Sáez-Benito MC, Álvarez Ballano D, de Arriba Muñoz A.

Med Clin (Barc). 2018 Jan 12;150(1):40-41. doi: 10.1016/j.medcli.2017.06.073. Epub 2017 Oct 7. English, Spanish. No abstract available.

PMID:
28992979
6.

[X-linked adrenoleukodystrophy: a report of three cases. The importance of early diagnosis].

López Úbeda M, de Arriba Muñoz A, Ferrer Lozano M, Labarta Aizpún JI, García Jiménez MC.

Arch Argent Pediatr. 2017 Oct 1;115(5):e279-e281. doi: 10.5546/aap.2017.e279. Spanish.

7.

New pathogenic variant in the NPR2 gene: Etiology of low size, macrocephaly and bone dysplasia in a male with acromesomelic dysplasia Maroteaux-type.

Vera Sáez-Benito MC, Izquierdo-Álvarez S, de Arriba Muñoz A.

Med Clin (Barc). 2017 Dec 20;149(12):553-554. doi: 10.1016/j.medcli.2017.06.012. Epub 2017 Jul 21. English, Spanish. No abstract available.

PMID:
28736064
8.

Heterozygous mutation in the receptor gene of the growth hormone as cause of short stature.

Barrio-Ollero E, Izquierdo-Álvarez S, de Arriba Muñoz A.

Med Clin (Barc). 2017 Jan 20;148(2):e9-e10. doi: 10.1016/j.medcli.2016.10.014. Epub 2016 Nov 30. English, Spanish. No abstract available.

PMID:
27914676
9.

[Sepsis due to Pseudomona as a debut of a primary immunodeficiency in a child].

Vera Sáez-Benito MC, López Úbeda M, Madurga Revilla P, de Arriba Muñoz A, Bustillo Alonso M, Rodríguez-Vigil Iturrate C.

Arch Argent Pediatr. 2016 Dec 1;114(6):e444-e447. doi: 10.5546/aap.2016.e444. Spanish.

10.

[Tuberculous hypophysitis mimicking Tolosa-Hunt syndrome].

Monge-Galindo L, De Arriba-Munoz A, Ubalde-Sainz E, Ferrer-Lozano M, Guerrero-Laleona C, Lopez-Pison J.

Rev Neurol. 2016 Sep 16;63(6):284-5. Spanish. No abstract available.

11.

Valores de normalidad de índice de masa corporal y perímetro abdominal en población española desde el nacimiento a los 28 años de edad.

De Arriba Muñoz A, López Úbeda M, Rueda Caballero C, Labarta Aizpún JI, Ferrández Longás Á.

Nutr Hosp. 2016 Jul 19;33(4):388. doi: 10.20960/nh.388. Spanish.

12.

Hypopituitarism: An uncommon cause of developmental delay.

López Úbeda M, de Arriba Muñoz A, Abenia Usón P, Labarta Aizpún JI.

Neurologia. 2018 Oct;33(8):551-552. doi: 10.1016/j.nrl.2016.05.013. Epub 2016 Jul 21. English, Spanish. No abstract available.

13.

[Growth hormone treatment in small for gestational age children in Spain].

Rial Rodríguez JM, de Arriba Muñoz A, Bosch Muñoz J, Cabanas Rodríguez P, Cañete Estrada R, Díez López I, Hawkins Solís MM, Martínez-Aedo Ollero MJ, Rodríguez Dehli AC, Ibáñez Toda L; en representación del Grupo de trabajo para el estudio del paciente pequeño para la edad gestacional (PEG) de la Sociedad Española de Endocrinología Pediátrica (SEEP).

An Pediatr (Barc). 2017 May;86(5):249-254. doi: 10.1016/j.anpedi.2016.04.001. Epub 2016 May 13. Spanish.

14.

[Human growth hormone and Turner syndrome].

Sánchez Marco SB, de Arriba Muñoz A, Ferrer Lozano M, Labarta Aizpún JI, Garagorri Otero JM.

An Pediatr (Barc). 2017 Feb;86(2):81-86. doi: 10.1016/j.anpedi.2016.02.009. Epub 2016 May 11. Spanish.

15.

[Importance of multidisciplinary monitoring in Medicine: CHARGE syndrome].

López Úbeda M, de Arriba Muñoz A, Labarta Aizpún JI.

Med Clin (Barc). 2016 Aug 5;147(3):135. doi: 10.1016/j.medcli.2016.02.008. Epub 2016 Mar 28. Spanish. No abstract available.

PMID:
27033434
16.

Is acute otitis media always banal? Clinical cases and review of intracranial complications.

Ruiz Del Olmo Izuzquiza I, de Arriba Muñoz A, Romero Gil R, López Pisón J.

Neurologia. 2016 Sep;31(7):496-8. doi: 10.1016/j.nrl.2014.12.013. Epub 2015 Feb 26. English, Spanish. No abstract available.

17.

[Hypogonadotropic hypogonadism in Klinefelter syndrome and hypothalamic-pituitary tumor].

Beisti Ortego A, De Arriba Muñoz A, Ferrer Lozano M, Martínez de Zabarte Fernández JM, Calvo Escribano C, Labarta Aizpún JI.

Arch Argent Pediatr. 2015 Jan;113(1):e6-9. doi: 10.1590/S0325-00752015000100011. Spanish.

18.

[Autosomal dominant osteopetrosis: a presentation of 3 cases and a new gene mutation].

Janer Subías E, de Arriba Muñoz A, García Iñiguez JP, Ferrer Lozano M, Sanchez Del Pozo J, Labarta Aizpun JI.

An Pediatr (Barc). 2015 Jan;82(1):e35-8. doi: 10.1016/j.anpedi.2014.03.014. Epub 2014 Jun 2. Spanish.

19.

[Congenital adrenal hyperplasia due to lack of 17α-hydroxylase: a report of a new mutation in the gene CYP17A1].

Perales Martínez JI, Pina Marqués B, de Arriba Muñoz A, Mayayo Dehesa E, Labarta Aizpún JI, Loidi Fernández L.

An Pediatr (Barc). 2015 Jan;82(1):e64-7. doi: 10.1016/j.anpedi.2013.11.019. Epub 2014 Mar 1. Spanish.

20.

[Type 1 polyglandular autoimmune syndrome associated with C322fsx372 mutation].

Roncalés-Samanes P, de Arriba Muñoz A, Lou Francés GM, Ferrer Lozano M, Justa Roldán ML, Labarta Aizpun JI.

An Pediatr (Barc). 2015 Jan;82(1):e60-3. doi: 10.1016/j.anpedi.2014.01.012. Epub 2014 Feb 26. Spanish.

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