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Pediatric urology surgical complications and management
Pediatric urology surgical complications and management
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Pediatric urology surgical complications and management

Duncan T Wilcox; Prasad Godbole; Martin A Koyle

Oxford, UK Wiley-Blackwell Hoboken, N.J 2008

Localização: FM - Fac. Medicina    (WG220 E21 2010 )(Acessar)

2
Zinner syndrome in children: clinical presentation, imaging findings, diagnosis, and outcome
Zinner syndrome in children: clinical presentation, imaging findings, diagnosis, and outcome
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Zinner syndrome in children: clinical presentation, imaging findings, diagnosis, and outcome

Lin, Chun-Chen ; Sheu, Jin-Cherng ; Tsai, Pei-Shan ; Lee, Ming-Dar ; Lin, Tsu-Hua ; Tsai, Jeng-Daw

Pediatric nephrology (Berlin, West), 2022-12, Vol.37 (12), p.3075-3084 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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3
Free Tube Graft Urethroplasty for Repair of Hypospadias
Free Tube Graft Urethroplasty for Repair of Hypospadias
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Free Tube Graft Urethroplasty for Repair of Hypospadias

Obara, Kenji ; Hoshii, Tatsuhiko  ; Hoshino, Sayaka ; Yamana, Kazutoshi  ; Anraku, Tsutomu ; Maruyama, Ryo ; Kuroki, Hiroo ; Ishizaki, Fumio  ; Yamazaki , Hiroyuki  ; Tomita, Yoshihiko

Urologia internationalis, 2020-06, Vol.104 (5-6), p.386-390 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

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4
Ultrasound as a Screening Test for Genitourinary Anomalies in Children With UTI
Ultrasound as a Screening Test for Genitourinary Anomalies in Children With UTI
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Ultrasound as a Screening Test for Genitourinary Anomalies in Children With UTI

NELSON, Caleb P ; JOHNSON, Emilie K ; LOGVINENKO, Tanya ; CHOW, Jeanne S

Pediatrics (Evanston), 2014-03, Vol.133 (3), p.394-403 [Periódico revisado por pares]

Elk Grove Village, IL: American Academy of Pediatrics

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5
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report
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Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report

Schierz, Ingrid Anne Mandy ; Giuffrè, Mario ; Cimador, Marcello ; D'Alessandro, Maria Michela ; Serra, Gregorio ; Favata, Federico ; Antona, Vincenzo ; Piro, Ettore ; Corsello, Giovanni

Italian journal of pediatrics, 2022-02, Vol.48 (1), p.19-19, Article 19 [Periódico revisado por pares]

England: BioMed Central

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6
Hemangioma of the scrotal septum: a rare entity in infants with review of the literature
Hemangioma of the scrotal septum: a rare entity in infants with review of the literature
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Hemangioma of the scrotal septum: a rare entity in infants with review of the literature

Kumar, Tarun ; Vaughan, Richard ; Dangle, Pankaj P

West Virginia medical journal, 2012-07, Vol.108 (4), p.26-27 [Periódico revisado por pares]

United States: West Virginia State Medical Association

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7
A single-center study to evaluate the efficacy of a fetal urine peptide signature predicting postnatal renal outcome in fetuses with posterior urethral valves
A single-center study to evaluate the efficacy of a fetal urine peptide signature predicting postnatal renal outcome in fetuses with posterior urethral valves
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A single-center study to evaluate the efficacy of a fetal urine peptide signature predicting postnatal renal outcome in fetuses with posterior urethral valves

Buffin-Meyer, Bénédicte ; Tkaczyk, Marcin ; Stańczyk, Małgorzata ; Breuil, Benjamin ; Siwy, Justyna ; Szaflik, Krzysztof ; Talar, Tomasz ; Wojtera, Justyna ; Krzeszowski, Waldemar ; Decramer, Stéphane ; Klein, Julie ; Schanstra, Joost P.

Pediatric nephrology (Berlin, West), 2020-03, Vol.35 (3), p.469-475 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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8
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
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HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort

Thomas, Rosemary ; Sanna-Cherchi, Simone ; Warady, Bradley A. ; Furth, Susan L. ; Kaskel, Frederick J. ; Gharavi, Ali G.

Pediatric nephrology (Berlin, West), 2011-06, Vol.26 (6), p.897-903 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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9
Genital anomalies in newborns
Genital anomalies in newborns
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Genital anomalies in newborns

Mecarini, Federico ; Fanos, Vassilios ; Crisponi, Giangiorgio

Journal of perinatology, 2021-09, Vol.41 (9), p.2124-2133 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Pediatric Urology: Surgical Complications and Management
Pediatric Urology: Surgical Complications and Management
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Livro 		Adicionar ao Meu Espaço

Pediatric Urology: Surgical Complications and Management

Godbole, Prasad P ; Koyle, Martin A ; Wilcox, Duncan T

Newark: Wiley 2015

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Deste Autor:

  1. Koyle, M
  2. Wilcox, D
  3. Godbole, P

Neste Assunto:

  1. Infant
  2. Genitourinary Organs
  3. Genitourinary Organs
  4. Infant
  5. Humans

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