T. Boemers

发表

Bladder exstrophy–epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients

C. Thauvin-Robinet, H. Reutter, W. Rösch, 2006, Scandinavian journal of urology and nephrology.

CNV analysis in 169 patients with bladder exstrophy-epispadias complex

M. Nöthen, S. Moebus, A. Brusco, 2016, BMC Medical Genetics.

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B

Da I Jung, M. Nöthen, I. V. van Rooij, 2022, HGG advances.

Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene.

M. Nöthen, H. Reutter, M. Ludwig, 2012, International journal of molecular medicine.

Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia

S. Heilmann-Heimbach, M. Lacher, Amit Sharma, 2020, PloS one.

Urodynamic evaluation of children with the caudal regression syndrome (caudal dysplasia sequence).

J. V. van Gool, T. D. de Jong, K. Bax, 1994, The Journal of urology.

Esophageal Atresia with or without Tracheoesophageal Fistula (EA/TEF): Association of Different EA/TEF Subtypes with Specific Co-occurring Congenital Anomalies and Implications for Diagnostic Workup

M. Lacher, J. Schumacher, B. Ure, 2017, European Journal of Pediatric Surgery.

Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.

M. Nöthen, J. Schumacher, N. Zwink, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Preliminary report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations.

S. Moore, B. Ure, A. Coran, 2005, Journal of pediatric surgery.

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.

M. Lacher, J. Schumacher, N. Zwink, 2016, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation

D. Tibboel, M. Lacher, N. Roeleveld, 2016, European Journal of Pediatrics.

A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy

I. V. van Rooij, D. Werring, J. Riancho, 2022, Communications Biology.

Traumatic Vulvar Epithelial Inclusion Cysts Following Female Genital Mutilation (FGM)

S. Banaschak, T. Boemers, B. Mack-Detlefsen, 2015, Geburtshilfe und Frauenheilkunde.

Assisted reproductive techniques and risk of exstrophy-epispadias complex: a German case-control study.

H. Brenner, N. Zwink, E. Jenetzky, 2013, The Journal of urology.

Lower urinary tract dysfunction in children with benign sacrococcygeal teratoma.

J. V. van Gool, T. D. de Jong, K. Bax, 1994, The Journal of urology.

The Cologne pouch procedure for continent anal urinary diversion in children with bladder exstrophy-epispadias complex.

T. Boemers, R. Vahdad, T. Klein, 2018, Journal of pediatric urology.

Lipschütz-Ulkus

K. Feld, S. Banaschak, T. Boemers, 2019, Rechtsmedizin.

Urinary incontinence and vesicourethral dysfunction in pediatric surgical conditions.

T. Boemers, 2002, Seminars in pediatric surgery.

Urologic problems in anorectal malformations. Part 1: Urodynamic findings and significance of sacral anomalies.

F. Beek, J. V. van Gool, T. D. de Jong, 1996, Journal of pediatric surgery.

Neonatal management of female intersex by clitorovaginoplasty.

T. D. de Jong, T. Boemers, 1995, The Journal of urology.

Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.

M. Nöthen, M. Lacher, N. Zwink, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Transient renal insufficiency by bilateral renal cysts and posterior urethral valves.

W. Barthlen, T. Boemers, G. Stuhldreier, 2002, Journal of pediatric surgery.

Urologic sequelae in sacrococcygeal teratoma

K. Bax, T. Boemers, 1993, Pediatric Surgery International.

Urologic problems in anorectal malformations. Part 2: functional urologic sequelae.

J. V. van Gool, T. D. de Jong, K. Bax, 1996, Journal of pediatric surgery.

Spine evaluation in children with anorectal malformations

W. Mali, M. V. van Leeuwen, F. Beek, 1995, Pediatric Radiology.

Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloaca

H. Reutter, M. Ludwig, T. Boemers, 2008, Pediatric Surgery International.

Dynamic magnetic resonance imaging of the pelvic floor in children and adolescents with vesical and anorectal malformations

R. Forstner, C. Schimke, B. Ludwikowski, 2006 .

Iatrogenic urethral strictures following pull-through procedures: buccal mucosa inlay repair.

D. Rohrmann, T. Boemers, 2005, Journal of pediatric urology.

The effect of rectosigmoidectomy and Duhamel-type pull-through procedure on lower urinary tract function in children with Hirschsprung's disease.

J. V. van Gool, T. Boemers, N. Bax, 2001, Journal of pediatric surgery.

The effect of posterior sagittal anorectoplasty and its variants on lower urinary tract function in children with anorectal malformations.

J. V. van Gool, K. Bax, M. Rövekamp, 1995, The Journal of urology.

Epidemiological survey of 214 families with bladder exstrophy-epispadias complex.

T. Höller, J. Gearhart, S. Boyadjiev, 2008, The Journal of urology.

De novo microduplication at 22q11.21 in a patient with VACTERL association.

M. Nöthen, S. Aretz, F. Brockschmidt, 2011, European journal of medical genetics.

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

M. Nöthen, S. Moebus, M. Mattheisen, 2015, PLoS genetics.

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

M. Nöthen, I. V. van Rooij, T. Becker, 2014, Human molecular genetics.

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula

D. Tibboel, M. Lacher, P. Hoffmann, 2016, European Journal of Human Genetics.

Multiple hepatic mesenchymal hamartomas in a premature associated with placental mesenchymal dysplasia.

P. Groneck, T. Boemers, R. Bald, 2011, Journal of pediatric surgery.

SLC20A1 Is Involved in Urinary Tract and Urorectal Development

I. V. van Rooij, W. Newman, M. Lacher, 2020, Frontiers in Cell and Developmental Biology.

Covered exstrophy associated with an anorectal malformation: A rare variant of classical bladder exstrophy

M. Rövekamp, T. Boemers, N. Bax, 1994, Pediatric Surgery International.

Prenatal Diagnosis of Covered Cloacal Exstrophy

M. Mallmann, U. Gembruch, H. Reutter, 2014, Fetal Diagnosis and Therapy.

Duplicate exstrophy

T. Boemers, T. Jong, P. Vegt, 1995, Pediatric Surgery International.

Concordance analyses of twins with bladder exstrophy–epispadias complex suggest genetic etiology

L. Qi, J. Gearhart, S. Boyadjiev, 2007, American journal of medical genetics. Part A.

Severe Vaginal Burns in a 5-Year-Old Girl Due to an Alkaline Battery in the Vagina.

T. Boemers, A. Semaan, M. R. Vahdad, 2015, Journal of pediatric and adolescent gynecology.

Experiences with LESS-appendectomy in Children.

G. Cernaianu, H. Foroutan, T. Boemers, 2016, Archives of Iranian medicine.

The Surgical Correction of Buried Penis: A New Technique

T. Boemers, T. Jong, 1995 .

Long-term health-related quality of life after complex and/or complicated esophageal atresia in adults and children registered in a German patient support group.

H. Till, B. Ure, B. Vaske, 2014, Journal of pediatric surgery.

Coincidence of congenital left-sided diaphragmatic hernia and ductus venosus agenesis: Relation between altered hemodynamic flow and lung-to-head-ratio?

R. Stressig, T. Boemers, A. Semaan, 2015 .

Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe.

M. Nöthen, J. Gearhart, S. Boyadjiev, 2011, The Journal of pediatrics.

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

M. Nöthen, S. Moebus, P. Hoffmann, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

A. Buness, S. Heilmann-Heimbach, M. Lacher, 2022, European Journal of Human Genetics.

Single-center outcome analysis of 46 fetuses with megacystis after intrauterine vesico-amniotic shunting with the Somatex®intrauterine shunt

L. Weber, M. Liebau, E. Weber, 2023, Archives of gynecology and obstetrics.

Quality of Life after Surgical Treatment for Esophageal Atresia: Long-Term Outcome of 154 Patients

M. Lacher, J. Schumacher, B. Ure, 2017, European Journal of Pediatric Surgery.

Ex-Utero Intrapartum Treatment (EXIT) in a giant case of Congenital Cystic Adenomatoid Malformation (CCAM) of the lung.

S. Ofner, R. Forstner, H. Steiner, 2007, Ultraschall in der Medizin.

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.

M. Nöthen, B. Herrmann, L. Wittler, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.

M. Nöthen, S. Moebus, P. Hoffmann, 2010, European journal of medical genetics.

An experimental study in six fresh human cadavers using a novel approach to avoid abdominal wall incisions in total colectomy: totally transanal laparoendoscopic single-site pull-through colectomy with J-pouch creation

S. Faran, G. Cernaianu, H. Foroutan, 2016, Surgical Endoscopy.

Urological problems after surgical treatment of scoliosis in children with myelomeningocele.

H. Pruijs, T. D. de Jong, T. Boemers, 1996, The Journal of urology.

The neuropathic bladder

T. Boemers, 2005 .

Stapled neoappendicostomy: A novel technique.

M. Wallis, M. Rollins, T. Boemers, 2022, Journal of Pediatric Surgery.

Colpo‐wrap: a new continence procedure

C. Schimke, T. Boemers, 2005, BJU international.

Treatment of enuresis risoria in children by self-administered electric and imaginary shock.

J. V. van Gool, M. Vijverberg, A. P. Messer, 1995, British journal of urology.

The surgical correction of buried penis: a new technique.

T. Boemers, T. D. de Jong, 1996, The Journal of urology.

MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?

R. Betz, H. Reutter, M. Ludwig, 2006, European Journal of Pediatrics.

Evaluation of urinary and faecal continent stomas.

C. Schimke, B. Ludwikowski, T. Boemers, 2005, Journal of pediatric urology.

Mitrofanoff procedure with Meckel's diverticulum

T. Boemers, 2001, BJU international.

PERSISTENT CLOACA: UROLOGICAL THERAPY

C. Schimke, T. Boemers, M. Ardelean, 2011 .

Tethered spinal cord: the effect of neurosurgery on the lower urinary tract and male sexual function

J. V. van Gool, T. D. de Jong, T. Boemers, 1995 .

Laparoscopic hepatopexy: a new surgical approach to hepatoptosis in an 11-year-old boy.

M. Dübbers, T. Boemers, C. Städtler, 2011, Journal of laparoendoscopic & advanced surgical techniques. Part A.

Necrotizing enterocolitis in premature twins with twin-to-twin transfusion syndrome.

C. Schimke, T. Boemers, B. Detlefsen, 2008, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Rotundum psoas hitch: a new method for colpohysteropexy in girls with bladder exstrophy.

C. Schimke, B. Ludwikowski, T. Boemers, 2005, Journal of pediatric urology.

Lymphnode tuberculosis in a 4-year-old boy with relapsed ganglioneuroblastoma: a case report

A. Borkhardt, M. Kuhlen, M. Ortmann, 2018, BMC Infectious Diseases.

Surgical Repair of a Superior Sternal Cleft in an Infant

T. Boemers, M. Kellner, B. Mack-Detlefsen, 2015, European Journal of Pediatric Surgery Reports.

Isolated bladder exstrophy in prenatal diagnosis

M. Mallmann, U. Gembruch, H. Reutter, 2019, Archives of Gynecology and Obstetrics.

Prenatal Diagnosis of Hydro(metro)colpos: A Series of 20 Cases

M. Mallmann, U. Gembruch, H. Reutter, 2018, Fetal Diagnosis and Therapy.

Can a simplified algorithm prevent incomplete laparoscopic pyloromyotomy?

G. Cernaianu, T. Boemers, A. Semaan, 2015, Journal of pediatric surgery.

Congenital obstructive distal urethral membrane.

C. Schimke, T. Boemers, B. Detlefsen, 2005, Journal of pediatric urology.

Neomycin toxicity in bladder irrigation.

T. D. de Jong, R. Donckerwolcke, T. Boemers, 1993, Journal of Urology.

De novo duplication of 18p11.21–18q12.1 in a female with anorectal malformation

P. Hoffmann, S. Aretz, A. Zink, 2011, American journal of medical genetics. Part A.

[Aphallia - report of two cases].

E. Korsch, T. Boemers, B. Mack-Detlefsen, 2020, Der Urologe. Ausg. A.

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

S. Heilmann-Heimbach, M. Lacher, F. Degenhardt, 2017, Birth defects research.

Possible association of Down syndrome and exstrophy–epispadias complex: report of two new cases and review of the literature

H. Reutter, W. Rösch, M. Ludwig, 2009, European Journal of Pediatrics.

Family‐based association study of the MTHFR polymorphism C677T in the bladder‐exstrophy‐epispadias‐complex

T. Becker, R. Betz, H. Reutter, 2006, American journal of medical genetics. Part A.

Association Between Exstrophy-epispadias Complex And Congenital Anomalies: A German Multicenter Study.

M. Lacher, N. Zwink, E. Jenetzky, 2019, Urology.