Pesquisa | BVS Integralidade em Saúde

1.

Peter's anomaly-A homeotic gene disorder.

Kylat, Ranjit I.

Acta Paediatr ; 111(5): 948-951, 2022 05.

Artigo em Inglês | MEDLINE | ID: mdl-35044009

2.

Mucolipidosis II.

Kylat, Ranjit I.

J Pediatr ; 229: 302-304, 2021 02.

Artigo em Inglês | MEDLINE | ID: mdl-33038345

3.

Immune dysregulation, polyendocrinopathy and enteropathy, X-linked (IPEX) syndrome due to a mutation in FOXP3, modified by a pathogenic variant in SON (SON DNA-binding protein).

Kylat, Ranjit I; Stanley, Kelly; Simon, Sarah; Erickson, Robert P.

J Appl Genet ; 64(1): 141-144, 2023 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-36175752

4.

An unusual presentation of neonatal rhabdomyosarcoma: a case report.

Strah, Danielle; Stanley, Kelly; Oatmen, Kelsie; Kylat, Ranjit I; Dishop, Megan; de la Maza, Michelina.

Front Pediatr ; 11: 1233334, 2023.

Artigo em Inglês | MEDLINE | ID: mdl-37964815

5.

Recombinant human activated protein C for severe sepsis in neonates.

Kylat, Ranjit I; Ohlsson, Arne.

Cochrane Database Syst Rev ; (4): CD005385, 2012 Apr 18.

Artigo em Inglês | MEDLINE | ID: mdl-22513930

6.

Neonatal testicular torsion.

Kylat, Ranjit I; Ahmed, Mohamed N.

Afr J Paediatr Surg ; 19(1): 1-4, 2022.

Artigo em Inglês | MEDLINE | ID: mdl-34916342

7.

A Truncating Variant of CHRNG as a Cause of Escobar Syndrome: A Multiple Pterygium Syndrome Subtype.

Sandweiss, Alexander J; Patel, Shalinkumar; Bader, Mohammad Y; Kylat, Ranjit I.

J Pediatr Genet ; 11(2): 144-146, 2022 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-35769964

8.

Pseudomonas aeruginosa necrotizing bronchopneumonia.

Kylat, Ranjit I.

Autops Case Rep ; 11: e2021271, 2021.

Artigo em Inglês | MEDLINE | ID: mdl-34307227

9.

Validity of Random Triglyceride Levels in Infants Receiving Parenteral Nutrition.

Bader, Mohammad Y; Lam, Melanie A; Munoz, Fernando; Thompson, Leslie; Kylat, Ranjit I.

Front Pediatr ; 9: 601915, 2021.

Artigo em Inglês | MEDLINE | ID: mdl-34222138

10.

A Retrospective Review Following the Addition of Clonidine to a Neonatal Abstinence Syndrome Treatment Algorithm.

Bader, Mohammad Y; Zaghloul, Nahla; Repholz, Ashley; Nagy, Nadia; Ahmed, Mohamed N; Thompson, Leslie; Kylat, Ranjit I.

Front Pediatr ; 9: 632836, 2021.

Artigo em Inglês | MEDLINE | ID: mdl-34164354

11.

Genetic Characterization of a Model Ciliopathy: Bardet-Biedl Syndrome.

Kops, Samantha A; Kylat, Ranjit I; Bhatia, Shanti; Seckeler, Michael D; Barber, Brent J; Bader, Mohammad Y.

J Pediatr Genet ; 10(2): 126-130, 2021 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-33996183

12.

Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease.

Kylat, Ranjit I.

Children (Basel) ; 7(9)2020 Aug 28.

Artigo em Inglês | MEDLINE | ID: mdl-32872114

13.

Caudal Regression Syndrome.

Kylat, Ranjit I; Bader, Mohammad.

Children (Basel) ; 7(11)2020 Nov 04.

Artigo em Inglês | MEDLINE | ID: mdl-33158301

14.

Junctional ectopic tachycardia in infants and children.

Kylat, Ranjit I; Samson, Ricardo A.

J Arrhythm ; 36(1): 59-66, 2020 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-32071621

15.

Unique Case of Congenital Duodenal Atresia and a Choledochal Cyst and the Hypothesis of Their Embryological Evolution.

Downing, Brittany; Bader, Mohammad Y; Morello, Frank P; Kylat, Ranjit I.

Children (Basel) ; 7(8)2020 Aug 18.

Artigo em Inglês | MEDLINE | ID: mdl-32824642

16.

Pneumomediastinum Mimicking Congenital Pulmonary Airway Malformation.

Kylat, Ranjit I.

Children (Basel) ; 6(9)2019 Sep 17.

Artigo em Inglês | MEDLINE | ID: mdl-31533336

17.

Complete and Incomplete Pentalogy of Cantrell.

Kylat, Ranjit I.

Children (Basel) ; 6(10)2019 Oct 06.

Artigo em Inglês | MEDLINE | ID: mdl-31590448

18.

Tracheal Stenosis and Congenital Heart Disease in Trisomy 21.

Kylat, Ranjit I.

Children (Basel) ; 6(9)2019 Sep 04.

Artigo em Inglês | MEDLINE | ID: mdl-31487969

19.

Pulmonary hypertension occurring with diazoxide use in a preterm infant with hypoglycemia.

Kylat, Ranjit I.

Drug Healthc Patient Saf ; 11: 7-10, 2019.

Artigo em Inglês | MEDLINE | ID: mdl-30881142

20.

Permanent junctional reciprocating tachycardia in infants and Children.

Kylat, Ranjit I; Samson, Ricardo A.

J Arrhythm ; 35(3): 494-498, 2019 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-31293698

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Peter's anomaly-A homeotic gene disorder.

Mucolipidosis II.

Immune dysregulation, polyendocrinopathy and enteropathy, X-linked (IPEX) syndrome due to a mutation in FOXP3, modified by a pathogenic variant in SON (SON DNA-binding protein).

An unusual presentation of neonatal rhabdomyosarcoma: a case report.

Recombinant human activated protein C for severe sepsis in neonates.

Neonatal testicular torsion.

A Truncating Variant of CHRNG as a Cause of Escobar Syndrome: A Multiple Pterygium Syndrome Subtype.

Pseudomonas aeruginosa necrotizing bronchopneumonia.

Validity of Random Triglyceride Levels in Infants Receiving Parenteral Nutrition.

A Retrospective Review Following the Addition of Clonidine to a Neonatal Abstinence Syndrome Treatment Algorithm.

Genetic Characterization of a Model Ciliopathy: Bardet-Biedl Syndrome.

Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease.

Caudal Regression Syndrome.

Junctional ectopic tachycardia in infants and children.

Unique Case of Congenital Duodenal Atresia and a Choledochal Cyst and the Hypothesis of Their Embryological Evolution.

Pneumomediastinum Mimicking Congenital Pulmonary Airway Malformation.

Complete and Incomplete Pentalogy of Cantrell.

Tracheal Stenosis and Congenital Heart Disease in Trisomy 21.

Pulmonary hypertension occurring with diazoxide use in a preterm infant with hypoglycemia.

Permanent junctional reciprocating tachycardia in infants and Children.