Aneiros Castro B, Cabezalí Barbancho D, Tordable Ojeda C, Carrillo Arroyo I, Redondo Sedano J, Gómez Fraile A. Laparoendoscopic single-site nephrectomy in children: Is it a good alternative to conventional laparoscopic approach? J Pediatr Urol. 2018;14(1):49.e1-49.e4.

Astigarraga I, González Granado LI, Allende LM, Alsina L. Síndrtomes hemofagocíticos: la importancia del diagnóstico y del tratamiento precoces. An Pediatr (Barc). 2018;89(2):124.e1-124.e8

Barrios A, Fernández Cooke E, Grasa C, Calvo C. Aneurismas coronarios gigantes en lactantes con enfermedad de Kawasaki. An Pediatr (Barc). 2018;88(3):178–9 [PubMed]

Barrios Tascón A, Centeno Malfaz F, Rojo Sombrero H, Fernández Cooke E, Sánchez Manubens J, Pérez-Lescure Picarzo J, et al. Consenso nacional sobre diagnóstico, tratamiento y seguimiento cardiológico de la enfermedad de Kawasaki. An Pediatr (Barc). 2018;89(3):188.e1-188.e22.

Brasil S, Leal F, Vega A, Navarrete R, Ecay MJ, Desviat LR, et al. Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants. Orphanet J Rare Dis. 2018;13(1):125.

Charbit Henrion F, Parlato M, Hanein S, Duclaux Loras R, Nowak J, Begue B, et al. Diagnostic yield of next-generation sequencing in very early-onset inflammatory bowel diseases: A multicenter study. J Crohns Colitis. 2018;12(9):1104-12 [doi]

Collaborative Initiative for Paediatric HIV Education and Research (CIPHER) Global Cohort Collaboration, Slogrove AL, Schomaker M, Davies M-A, Williams P, Balkan S, et al. The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis. PLoS Med. 2018;15(3):e1002514 [PubMed]

De Inocencio J, Antón J, Calvo Penades I, Mesa del Castillo Bermejo P, Alcobendas R, Boteanu AL, et al. The Castilian Spanish version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR). Rheumatol Int. 2018;38(Suppl 1):91-8

De la Oliva P, Cambra Lasaosa FJ, Quintana Díaz M, Rey Galán C, Sánchez Díaz JI, Martín Delgado MC, et al. Admission, discharge and triage guidelines for paediatric intensive care units in Spain. Med Intensiva. 2018;42(4):235-46

De la Oliva P, Cambra Lasaosa FJ, Quintana Díaz M, Rey Galán C, Sánchez Díaz JI, Martín Delgado MC, et al. Guías de ingreso, alta y triage para las unidades de cuidados intensivos pediátricos en España. An Pediatr (Barc). 2018;88(5):287.e1–287.e11 [PubMed]

Diab Cáceres L, Girón Moreno RM, Pastor Sanz MT, Quintana Gallego E, Delgado Pecellín I, Blanco Aparicio M, et al. Compassionate use of Lumacaftor/Ivacaftor in cystic fibrosis: Spanish experience. Arch Bronconeumol. 2018;54(12):614-8

Domínguez Pinilla N, Allende LM, Rosaín J, Gallego MDC, Chaves F, Deswarte C, et al. Disseminated abscesses due to Mycoplasma faucium in a patient with activated PI3Kδ syndrome type 2. J Allergy Clin Immunol Pract. 2018;6(5):1796-1798.e2 [PubMed]

European Pregnancy and Paediatric HIV Cohort Collaboration (EPPICC) study group in EuroCoord, Judd A, Chappell E, Turkova A, Le Coeur S, Noguera-Julian A, et al. Long-term trends in mortality and AIDS-defining events after combination ART initiation among children and adolescents with perinatal HIV infection in 17 middle- and high-income countries in Europe and Thailand: A cohort study. PLoS Med. 2018;15(1):e1002491 [PubMed]

Friedrich P, Guerra García P, Stetson A, Duncan C, Lehmann L. Young female donors do not increase the risk of graft-versus-host disease or impact overall outcomes in pediatric HLA-matched sibling hematopoietic stem cell transplantation. Biol Blood Marrow Transplant. 2018;24(1):96–102 [PubMed]

García Aranda B, Sarnago F, Velázquez MT, Mendoza A, López Gude MJ, Alonso González R. Selection of the Best of 2017 in Congenital Heart Disease. Rev Esp Cardiol (Engl Ed). 2018;71(4):302-3

González Granado LI, Ruiz García R, Blas Espada J, Moreno Villares JM, Germán Diaz M, López Nevado M, et al. Acquired and innate immunity impairment and severe disseminated mycobacterium genavense infection in a patient with a NF-κB1 deficiency. Front Immunol. 2018;9:3148

González Tomé MI, García López-Hortelano M, Fregonese L. Luces y sombras en la transmisión vertical de la enfermedad de Chagas. An Pediatr (Barc). 2018;88(3):119–21 [PubMed]

Llanos Alonso N, Epalza Ibarrondo C, Carretero Vicario O, Prieto Tato LM. A 7-year-old boy with preseptal cellulitis of torpid evolution. Enferm Infecc Microbiol Clin. 2018;36(10):662-3

Madrid L, Maculuve SA, Vilajeliu A, Sáez E, Massora S, Cossa A, et al. Maternal Carriage of Group B Streptococcus and Escherichia coli in a District Hospital in Mozambique. Pediatr Infect Dis J. 2018;37(11):1145-53

Malagón C, Mosquera Pongutà AC, De Inocencio J, Consolaro A, Bovis F, Ruperto N, et al. The Colombian Spanish version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR). Rheumatol Int. 2018;38(Suppl 1):107-13

Martin CA, Sarlós K, Logan CV, Thakur RS, Parry DA, Bizard AH, et al. Mutations in TOP3A cause a bloom syndrome-like disorder. Am J Hum Genet. 2018;103(2):221-31.

Martín Hernández E, Martínez Azorín F. Author’s Reply: TK2-related myopathic mitochondrial depletion syndrome. Pediatr Dev Pathol. 2018;21(5):509-10.

Martín Hernández E, Rodríguez García ME, Chen CA, Cotrina Vinagre FJ, Carnicero Rodríguez P, Bellusci M, et al. Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation. J Hum Genet. 2018;63(4):525-8

Martín Rivada Á, Rodríguez Contreras FJ, Muñoz Calvo MT, Güemes M, González Casado I, Del Pozo JS, et al. A novel GLI2 mutation responsible for congenital hypopituitarism and polymalformation syndrome. Growth Horm IGF Res. 2018;44:17-9

Martínez Rubioa A, Cortés Rico O, Pallás Alonso CR, Rando Diego Á, Sánchez Ruiz-Cabello FJ, Colomer Revuelta J, et al. Resumen infancia y adolescencia. Actualización PAPPS 2018. Aten Primaria. 2018;50:147-52

Martinón Torres F, Bernatowska E, Shcherbina A, Esposito S, Szenborn L, Marti MC, et al. Meningococcal B vaccine immunogenicity in children with defects in complement and splenic function. Pediatrics. 2018;142(3).

Martinón Torres F, Carmona Martinez A, Simkó R, Infante Marquez P, Arimany JL, Giménez Sánchez F, et al. Antibody persistence and booster responses 24-36 months after different 4CMenB vaccination schedules in infants and children: A randomised trial. J Infect. 2018;76(3):258–69 [PubMed]

McMillan HJ, Telegrafi A, Singleton A, Cho MT, Lelli D, Lynn FC, et al. Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy. Orphanet J Rare Dis. 2018;13(1):86

Mencía S, Palacios A, García M, Llorente AM, Ordóñez O, Toledo B, et al. An exploratory study of sevoflurane as an alternative for difficult sedation in critically ill children. Pediatr Crit Care Med. 2018;19(7):e335-e341 [PubMed]

Merinero B, Alcaide P, Martín Hernández E, Morais A, García Silva MT, Quijada Fraile P, et al. Four years’ experience in the diagnosis of very long-chain Acyl-CoA dehydrogenase deficiency in infants detected in three Spanish Newborn Screening Centers. JIMD Rep. 2018;39:63-74.

Moraleda C, Benmessaoud R, Esteban J, López Y, Alami H, Barkat A, et al. Prevalence, antimicrobial resistance and serotype distribution of group B streptococcus isolated among pregnant women and newborns in Rabat, Morocco. J Med Microbiol. 2018;67(5):652-61 [PubMed]

Moya CM, Zaballos MA, Garzón L, Luna C, Simón R, Yaffe MB, et al. TAZ/WWTR1 mediates the pulmonary effects of NKX2-1 mutations in brain-lung-thyroid syndrome. J Clin Endocrinol Metab. 2018;103(3):839-52 [PubMed]

Navarro Abia V, Soriano Ramos M, Núñez Enamorado N, Camacho Salas A, Martínez de Aragón A, Martín Hernández E, et al. Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review. Brain Dev. 2018;40(4):348–52 [PubMed]

Núñez Ramos R, Montoro S, Bellusci M, Del Fresno Valencia MR, Germán Díaz M, Urruzuno P, et al. Acute liver failure: Outcome and value of pediatric end-stage liver disease score in pediatric cases. Pediatr Emerg Care. 2018;34(6):409-12

Oulego Erroz I, González Cortés R, García Soler P, Balaguer Gargallo M, Frías Pérez M, Mayordomo Colunga J, et al. Ultrasound-guided or landmark techniques for central venous catheter placement in critically ill children. Intensive Care Med. 2018;44(1):61–72 [PubMed]

Pinto A, Adams S, Ahring K, Allen H, Almeida MF, García Arenas D, et al. Early feeding practices in infants with phenylketonuria across Europe. Mol Genet Metab Rep. 2018;16:82–9

Recio MJ, Domínguez Pinilla N, Perrig MS, Rodríguez Vigil-Iturrate C, Salmón Rodríguez N, Martínez Faci C, et al. Extreme phenotypes with identical mutations: Two patients with same non-sense NHEJ1 homozygous mutation. Front Immunol. 2018;9:2959

Rodríguez García ME, Cotrina Vinagre FJ, Cruz Rojo J, Garzón Lorenzo L, Carnicero Rodríguez P, Pozo JS-D, et al. A rare male patient with Fontaine progeroid syndrome caused by p.R217H de novo mutation in SLC25A24. Am J Med Genet A. 2018;176(11):2479-86

Rowe JH, Delmonte OM, Keles S, Stadinski BD, Dobbs AK, Henderson LA, et al. Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function. Blood. 2018;131(21):2335-44.

Ruiz Contreras J, Del Amo M, Picazo J. Effects of 13-valent pneumococcal conjugate vaccine on invasive pneumococcal disease in infants aged 0 to 90 days in Madrid, Spain. J Pediatric Infect Dis Soc. 2018;7(2):175-6

Santiago García B, Mellado Peña MJ, Baquero Artigao F, Contreras JR. Re: “Mycobacterial Disease in Immunocompromised Children in a High Endemic Area.” Pediatr Infect Dis J. 2018;37(4):376 [PubMed]

Sierra García P, López Maestro M, Torres Valdivieso MJ, Díaz González C, Carrasco M, Ares Segura S, et al. Developmental outcomes, attachment and parenting: Study of a sample of Spanish premature children. Span J Psychol. 2018;21:E20

Slack J, Albert MH, Balashov D, Belohradsky BH, Bertaina A, Bleesing J, et al. Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders. J Allergy Clin Immunol. 2018;141(1):322–8.e10 [PubMed]

Solana Gracia R, Rueda F, Betrián P, Gutiérrez Larraya F, Del Cerro MJ, Pan M, et al. Pediatrics Spanish Registry of Percutaneous Melody Pulmonary Valve Implantation in patients younger than 18 years. Rev Esp Cardiol (Engl Ed). 2018;71(4):283-90 [PubMed]

Soler Palacín P, De Gracia J, González Granado LI, Martín C, Rodríguez Gallego C, Sánchez Ramón S, et al. Primary immunodeficiency diseases in lung disease: warning signs, diagnosis and management. Respir Res. 2018;19(1):219

Soriano Ramos M, Navarro Abia V, Enamorado NN, Camacho Salas A, De Aragón AM, García Hoyos M, et al. Steroids for familial acute necrotizing encephalopathy: A future investment? Clin Neurol Neurosurg. 2018;174:134-6.

Soriano Ramos M, Núñez Enamorado N, Navarro Abia V, Simón de Las Heras R. Lactante con tortícolis aguda al despertar. An Pediatr (Barc). 2018;88(3):174–5 [PubMed]

Tagarro A, Chan M, Zangari P, Ferns B, Foster C, De Rossi A, et al. Early and highly suppressive antiretroviral therapy are main factors associated with low viral reservoir in european perinatally HIV-infected children. J Acquir Immune Defic Syndr. 2018;79(2):269-76

Varnier GC, Rosina S, Ferrari C, Pistorio A, Consolaro A, Bovis F, et al. Development and Testing of a Hybrid Measure of Muscle Strength in Juvenile Dermatomyositis for Use in Routine Care. Arthritis Care Res (Hoboken). 2018;70(9):1312-9.

Villafuerte B, Natera de Benito D, González A, Mori MA, Palomares M, Nevado J, et al. The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. Eur J Med Genet. 2018;61(7):393-8 [PubMed]

Zangari P, Palma P, Cotugno N, Rojo P, Tagarro A, Pepponi I, et al. Report from the First EPIICAL (Early-treated Perinatally HIV-infected Individuals: Improving Children’s Actual Life with Novel Immunotherapeutic Strategies) General Assembly meeting, 9-11 November 2017, Rome, Italy. J Virus Erad. 2018;4(1):51-4 [PubMed]