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Ilio‐inguinal‐transversus abdominis plane (I‐TAP) nerve block for elective caesarean section

Anaesthesia, 2018-10, Vol.73 (10), p.1295-1295

Gucev, G.

2018

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(137) Addition of Intrathecal Morphine to Manage Postoperative Pain in Pediatric Spine Surgery: A Meta-Analysis of Existing Studies

The journal of pain, 2019-04, Vol.20 (4), p.S10-S11

2019

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Bilateral Ultrasound-Guided Continuous Ilioinguinal-Iliohypogastric Block for Pain Relief After Cesarean Delivery

Anesthesia and analgesia, 2008-04, Vol.106 (4), p.1220-1222

2008

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TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis

The New England journal of medicine, 2015-01, Vol.372 (4), p.341-350

2015

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Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum

American journal of medical genetics. Part A, 2014-07, Vol.164A (7), p.1713-1733

2014

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Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature

Balkan journal of medical genetics, 2019-08, Vol.22 (1), p.81-88

2019

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Characteristic diagnostic clues of metatropic dysplasia: The lumbothoracic humpback with dumbbell appearance of the long bones

Balkan journal of medical genetics, 2018-12, Vol.21 (2), p.35-38

2018

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Rare heterozygous GDF6 variants in patients with renal anomalies

European journal of human genetics : EJHG, 2020-12, Vol.28 (12), p.1681-1693

2020

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Treatment and long-term outcome in primary distal renal tubular acidosis

Nephrology, dialysis, transplantation, 2019-06, Vol.34 (6), p.981-991

2019

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Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1097-E1103

2014

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Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

American journal of human genetics, 2012-12, Vol.91 (6), p.987-997

2012

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Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2

Human genetics, 2023-01, Vol.142 (1), p.73-88

2023

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Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux

Journal of the American Society of Nephrology, 2021-04, Vol.32 (4), p.805-820

2021

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Mutations in DSTYK and Dominant Urinary Tract Malformations

The New England journal of medicine, 2013-08, Vol.369 (7), p.621-629

2013

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Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology, 2023-06, Vol.34 (6), p.1105-1119

2023

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Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty

Journal of pediatric endocrinology & metabolism : JPEM, 2014-01, Vol.27 (1-2), p.199

2014

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Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder

American journal of medical genetics. Part A, 2008-10, Vol.146A (20), p.2688-2690

2008

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Insulin-like growth factor binding protein 3 mediates retinoic acid- and transforming growth factor β2-induced growth inhibition in human breast cancer cells

Cancer research (Chicago, Ill.), 1996-04, Vol.56 (7), p.1545-1550

1996

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Insulin-like growth factor-binding proteins (IGFBPs) and their regulatory dynamics

International Journal of Biochemistry and Cell Biology, 1996-06, Vol.28 (6), p.619-637

1996

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Aldosterone synthase deficiency type II with hypospadias

Indian pediatrics, 2012-04, Vol.49 (4), p.318-320

2012

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Response to "CLOVE(S) Syndrome: Expanding the Acronym"

American journal of medical genetics. Part A, 2009-02, Vol.149A (2), p.295-295

2009

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Aseptic necrosis of both tali in a child with steroid-dependent nephrotic syndrome

Nephrology, dialysis, transplantation, 2006-06, Vol.21 (6), p.1702-1704

2006

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Evidence for insulin-like growth factor (IGF)-independent transcriptional regulation of IGF binding protein-3 by growth hormone in SKHEP-1 human hepatocarcinoma cells

Endocrinology (Philadelphia), 1997-04, Vol.138 (4), p.1464-1470

1997

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Ilio‐inguinal‐transversus abdominis plane (I‐TAP) nerve block for elective caesarean section

(137) Addition of Intrathecal Morphine to Manage Postoperative Pain in Pediatric Spine Surgery: A Meta-Analysis of Existing Studies

Bilateral Ultrasound-Guided Continuous Ilioinguinal-Iliohypogastric Block for Pain Relief After Cesarean Delivery

TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis

Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum

Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature

Characteristic diagnostic clues of metatropic dysplasia: The lumbothoracic humpback with dumbbell appearance of the long bones

Rare heterozygous GDF6 variants in patients with renal anomalies

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA

Treatment and long-term outcome in primary distal renal tubular acidosis

Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux

Mutations in DSTYK and Dominant Urinary Tract Malformations

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty

Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder

Insulin-like growth factor binding protein 3 mediates retinoic acid- and transforming growth factor β2-induced growth inhibition in human breast cancer cells

Insulin-like growth factor-binding proteins (IGFBPs) and their regulatory dynamics

Aldosterone synthase deficiency type II with hypospadias

Response to "CLOVE(S) Syndrome: Expanding the Acronym"

Aseptic necrosis of both tali in a child with steroid-dependent nephrotic syndrome

Evidence for insulin-like growth factor (IGF)-independent transcriptional regulation of IGF binding protein-3 by growth hormone in SKHEP-1 human hepatocarcinoma cells

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