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Reprogramming of human fibroblasts toward a cardiac fate

Proceedings of the National Academy of Sciences - PNAS, 2013-04, Vol.110 (14), p.5588-5593

2013

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Evaluation and Treatment of Cryptorchidism: AUA Guideline

The Journal of urology, 2014-08, Vol.192 (2), p.337-345

2014

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Diagnosing Testicular Torsion before Urological Consultation and Imaging: Validation of the TWIST Score

The Journal of urology, 2016-06, Vol.195 (6), p.1870-1876

2016

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PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome

Nature communications, 2024-01, Vol.15 (1), p.339-339, Article 339

2024

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Urethral luminal epithelia are castration‐insensitive cells of the proximal prostate

The Prostate, 2020-08, Vol.80 (11), p.872-884

2020

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Medical and dietary interventions for preventing recurrent urinary stones in children

Cochrane database of systematic reviews, 2017-11, Vol.11 (11), p.CD011252

2017

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The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction

Prenatal diagnosis, 2024-02, Vol.44 (2), p.196-204

2024

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Contemporary review of testicular torsion: New concepts, emerging technologies and potential therapeutics

Journal of pediatric urology, 2013-12, Vol.9 (6), p.723-730

2013

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An Approach to the Identification of Anomalies and Etiologies in Neonates with Identified or Suspected VACTERL (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula with Esophageal Atresia, Cardiac Anomalies, Renal Anomalies, and Limb Anomalies) Association

The Journal of pediatrics, 2014-03, Vol.164 (3), p.451-457.e1

2014

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Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene

BMC medical genetics, 2020-02, Vol.21 (1), p.38-38, Article 38

2020

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SCGN deficiency results in colitis susceptibility

eLife, 2019-10, Vol.8

2019

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Bidirectional signaling mediated by ephrin-B2 and EphB2 controls urorectal development

Developmental biology, 2004-07, Vol.271 (2), p.272-290

2004

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Insulin-Like Peptide 3 (INSL3) Serum Concentration During Human Male Fetal Life

Frontiers in endocrinology (Lausanne), 2019-09, Vol.10, p.596-596

2019

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Author Reply to “Letter to the Editor on: Bladder Agenesis and Associated Pelvic Arterial Anomaly in 2 Female Pediatric Patients” (#URL-D-19-00427)

Urology (Ridgewood, N.J.), 2019-07, Vol.129, p.238-239

2019

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Bladder Agenesis and Associated Pelvic Arterial Anomaly in 2 Female Pediatric Patients

Urology (Ridgewood, N.J.), 2019-01, Vol.123, p.227-229

2019

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Genital Tubercles, Urethrogenesis and the Genital Organizer

The Journal of urology, 2016-10, Vol.196 (4), p.983-984

Baker, Linda A

2016

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Papers presented at the fall 2020 Pediatric Urologic Oncology Work Group of the Societies of Pediatric Urology meetingNeonatal Serum Electrolyte and Proteinuria Screening on 46,XY Ambiguous Genitalia Patients May Allow Early Diagnosis of Denys-Drash Syndrome: A Case Report

Urology (Ridgewood, N.J.), 2021-07, Vol.153, p.312-316

2021

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Dimensions of Reading Motivation and Their Relation to Reading Behavior and Competence

Reading research quarterly, 2012-10, Vol.47 (4), p.427-463

2012

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An analysis of clinical outcomes using color doppler testicular ultrasound for testicular torsion

Pediatrics (Evanston), 2000-03, Vol.105 (3 Pt 1), p.604

2000

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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.540-546

2011

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Pediatric Testicular Torsion: Demographics of National Orchiopexy Versus Orchiectomy Rates

The Journal of urology, 2011-06, Vol.185 (6), p.2459-2463

2011

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2020 INSL3 RECEPTOR RXFP2 IS EXPRESSED ON THE SPERM ACROSOME

The Journal of urology, , Vol.185 (4), p.e807-e808

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Urologic manifestations of hypotonia, ataxia, and delayed development syndrome (HADDS), a rare neurodevelopmental disorder

Journal of pediatric urology, 2023-12, Vol.19 (6), p.751.e1-751.e9

2023

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Modern management of and update on prune belly syndrome

Journal of pediatric urology, 2021-08, Vol.17 (4), p.548-554

2021

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UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients

American journal of medical genetics. Part A, 2010-12, Vol.152A (12), p.3084-3090

2010

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Reprogramming of human fibroblasts toward a cardiac fate

Evaluation and Treatment of Cryptorchidism: AUA Guideline

Diagnosing Testicular Torsion before Urological Consultation and Imaging: Validation of the TWIST Score

PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome

Urethral luminal epithelia are castration‐insensitive cells of the proximal prostate

Medical and dietary interventions for preventing recurrent urinary stones in children

The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction

Contemporary review of testicular torsion: New concepts, emerging technologies and potential therapeutics

An Approach to the Identification of Anomalies and Etiologies in Neonates with Identified or Suspected VACTERL (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula with Esophageal Atresia, Cardiac Anomalies, Renal Anomalies, and Limb Anomalies) Association

Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene

SCGN deficiency results in colitis susceptibility

Bidirectional signaling mediated by ephrin-B2 and EphB2 controls urorectal development

Insulin-Like Peptide 3 (INSL3) Serum Concentration During Human Male Fetal Life

Author Reply to “Letter to the Editor on: Bladder Agenesis and Associated Pelvic Arterial Anomaly in 2 Female Pediatric Patients” (#URL-D-19-00427)

Bladder Agenesis and Associated Pelvic Arterial Anomaly in 2 Female Pediatric Patients

Genital Tubercles, Urethrogenesis and the Genital Organizer

Papers presented at the fall 2020 Pediatric Urologic Oncology Work Group of the Societies of Pediatric Urology meetingNeonatal Serum Electrolyte and Proteinuria Screening on 46,XY Ambiguous Genitalia Patients May Allow Early Diagnosis of Denys-Drash Syndrome: A Case Report

Dimensions of Reading Motivation and Their Relation to Reading Behavior and Competence

An analysis of clinical outcomes using color doppler testicular ultrasound for testicular torsion

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

Pediatric Testicular Torsion: Demographics of National Orchiopexy Versus Orchiectomy Rates

2020 INSL3 RECEPTOR RXFP2 IS EXPRESSED ON THE SPERM ACROSOME

Urologic manifestations of hypotonia, ataxia, and delayed development syndrome (HADDS), a rare neurodevelopmental disorder

Modern management of and update on prune belly syndrome

UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients

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