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Items: 1 to 20 of 224


A case of atypical systemic primary carnitine deficiency in Saudi Arabia.

Alghamdi A, Almalki H, Shawli A, Waggass R, Hakami F.

Pediatr Rep. 2018 Jun 27;10(2):7705. doi: 10.4081/pr.2018.7705. eCollection 2018 May 24.


Rapunzel syndrome: how to orient the diagnosis.

Finale E, Franceschini P, Danesino C, Barbaglia M, Guala A.

Pediatr Rep. 2018 Jun 27;10(2):7689. doi: 10.4081/pr.2018.7689. eCollection 2018 May 24.


Takayasu arteritis with an initial presentation of chronic monoarthritis mimicking oligoarticular juvenile idiopathic arthritis.

Sukharomana M, Viravan S, Piyaphanee N, Charuvanij S.

Pediatr Rep. 2018 Jul 9;10(2):7648. doi: 10.4081/pr.2018.7648. eCollection 2018 May 24.


Waardenburg syndrome with isolated deficiency of myenteric ganglion cells at the sigmoid colon and rectum.

Watanabe S, Matsudera S, Yamaguchi T, Tani Y, Ogino K, Nakajima M, Yamaguchi S, Sasaki K, Suzumura H, Tsuchioka T.

Pediatr Rep. 2018 May 24;10(2):7500. doi: 10.4081/pr.2018.7500. eCollection 2018 May 24.


Isolated tubal torsion: A rare cause of acute abdomen in childhood.

Demirel BD, Hancioglu S, Bicakci U, Ariturk E, Bernay F.

Pediatr Rep. 2018 Apr 3;10(1):7604. doi: 10.4081/pr.2018.7604. eCollection 2018 Mar 22.


Anesthesia in Mowat-Wilson syndrome: information on 11 Italian patients.

Spunton M, Garavelli L, Mainardi PC, Emmig U, Finale E, Guala A.

Pediatr Rep. 2018 Mar 29;10(1):7514. doi: 10.4081/pr.2018.7514. eCollection 2018 Mar 22.


Acute encephalopathy with biphasic seizures and late reduced diffusion associated with Streptococcus sanguinis sepsis.

Awaguni H, Shinozuka J, Tanaka SI, Kadowaki S, Makino S, Maruyama R, Shigematsu Y, Hamaoka K, Imashuku S.

Pediatr Rep. 2018 Mar 29;10(1):7424. doi: 10.4081/pr.2018.7424. eCollection 2018 Mar 22.


An infantile alantoaxial dislocation with patent foramen ovale managed with titanium cabling and allogenic bone grafts.

Richard SA, Lan ZG, Yang X, Huang S.

Pediatr Rep. 2018 Mar 22;10(1):7339. doi: 10.4081/pr.2018.7339. eCollection 2018 Mar 22.


Epidemiology of vertebral fractures in pediatric and adolescent patients.

Saul D, Dresing K.

Pediatr Rep. 2018 Mar 29;10(1):7232. doi: 10.4081/pr.2018.7232. eCollection 2018 Mar 22.


A boy with recurrent swelling of the jaw.

Haverals L, Mattheij M, Hoppenreijs E, Bergé S, van der Weij A.

Pediatr Rep. 2018 Jan 4;9(4):7489. doi: 10.4081/pr.2017.7489. eCollection 2017 Nov 21. No abstract available.


Zika virus infection in a pediatric patient with acute gastrointestinal involvement.

Slavov S, Matsuno A, Yamamoto A, Otaguiri K, Cervi M, Covas D, Kashima S.

Pediatr Rep. 2018 Jan 3;9(4):7341. doi: 10.4081/pr.2017.7341. eCollection 2017 Nov 21. No abstract available.


Zinc supplementation enhances linear growth in school-aged children: A randomized controlled trial.

Rerksuppaphol S, Rerksuppaphol L.

Pediatr Rep. 2018 Jan 4;9(4):7294. doi: 10.4081/pr.2017.7294. eCollection 2017 Nov 21. No abstract available.


Pectus updates and special considerations in Marfan syndrome.

Fraser S, Child A, Hunt I.

Pediatr Rep. 2018 Jan 4;9(4):7277. doi: 10.4081/pr.2017.7227. eCollection 2017 Nov 21. No abstract available.


Initiation of complementary feeding and associated factors among children of age 6-23 months in Sodo town, Southern Ethiopia: Cross-sectional study.

Chane T, Bitew S, Mekonnen T, Fekadu W.

Pediatr Rep. 2018 Jan 3;9(4):7240. doi: 10.4081/pr.2017.7240. eCollection 2017 Nov 21. No abstract available.


46,XY ovotesticular disorders of sex development: A therapeutic challenge.

Scarpa MG, Grazia MD, Tornese G.

Pediatr Rep. 2017 Dec 11;9(4):7085. doi: 10.4081/pr.2017.7085. eCollection 2017 Nov 21. No abstract available.


Medium chain acyl-CoA dehydrogenase deficiency in a premature infant.

Dobrowolski SF, Ghaloul-Gonzalez L, Vockley J.

Pediatr Rep. 2017 Nov 21;9(4):7045. doi: 10.4081/pr.2017.7045. eCollection 2017 Nov 21.


The role of interleukin-6 in the early diagnosis of sepsis in premature infants.

Mirzarahimi M, Barak M, Eslami A, Enteshari-Moghaddam A.

Pediatr Rep. 2017 Oct 6;9(3):7305. doi: 10.4081/pr.2017.7305. eCollection 2017 Oct 6.


Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins.

Olivieri C, Mondino A, Chinello M, Risso A, Finale E, Lanciotti M, Guala A.

Pediatr Rep. 2017 Oct 6;9(3):7301. doi: 10.4081/pr.2017.7301. eCollection 2017 Oct 6.


Congenital vitiligo: A case observed in the cohort of HIV-exposed infants in Bobo-Dioulasso, Burkina Faso.

Barro M, Diallo JW, Ouattara ABI, Nacro B.

Pediatr Rep. 2017 Oct 6;9(3):7300. doi: 10.4081/pr.2017.7300. eCollection 2017 Oct 6.


Cystic intra-abdominal masses in children.

Ferrero L, GuanĂ  R, Carbonaro G, Cortese MG, Lonati L, Teruzzi E, Schleef J.

Pediatr Rep. 2017 Oct 6;9(3):7284. doi: 10.4081/pr.2017.7284. eCollection 2017 Oct 6.

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