Search Results - "Reutter HM"

AUTHOR REPLY.

Authors: Ebert AK Zwink N Reutter HM

Source: Urology [Urology] 2019 Jan; Vol. 123, pp. 219-220.

Publication Type: Journal Article; Comment

Journal Info: Publisher: Elsevier Science Country of Publication: United States NLM ID: 0366151 Publication Model: Print Cited Medium: Internet ISSN: 1527-9995 (Electronic) Linking ISSN: 00904295 NLM ISO Abbreviation: Urology Subsets: PubMed not MEDLINE

Long-term risk of renal impairment after complete primary repair of classic bladder exstrophy.

Authors: Eldin, Mohamed Emad Shahat, Ahmed A. Elderwy, Ahmed A. et al.

Source: Urology Annals. Apr-Jun2026, Vol. 18 Issue 2, p179-185. 7p.

Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract.

Authors: Vendrig, Lisanne M. ten Hoor, Mayke A. C. König, Benthe H. et al.

Source: Pediatric Nephrology. Mar2025, Vol. 40 Issue 3, p685-699. 15p.

Centralization as the key survival benefit in acute neonatal surgery.

Authors: Besendörfer M Günster S Linz K et al.

Source: Frontiers in pediatrics [Front Pediatr] 2024 Mar 14; Vol. 12, pp. 1382000. Date of Electronic Publication: 2024 Mar 14 (Print Publication: 2024).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE

Epispadias, a correctable cause of structural infertility in a middle-aged man: a case report.

Authors: Kura, Mustapha Abdulsalam, Khalifa Ibrahim Ayodeji, Afolayan et al.

Source: African Journal of Urology. 9/28/2024, Vol. 30 Issue 1, p1-4. 4p.

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

Authors: Mingardo, Enrico Beaman, Glenda Grote, Philip et al.

Source: Communications Biology. 11/9/2022, Vol. 5 Issue 1, p1-11. 11p.

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

Authors: Kalanithy JC Mingardo E Stegmann JD et al.

Source: Journal of medical genetics [J Med Genet] 2025 Jan 27; Vol. 62 (2), pp. 126-137. Date of Electronic Publication: 2025 Jan 27.

Publication Type: Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants.

Authors: Qiao L Welch CL Hernan R et al.

Source: American journal of human genetics [Am J Hum Genet] 2024 Nov 07; Vol. 111 (11), pp. 2362-2381. Date of Electronic Publication: 2024 Sep 26.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

SALL4 deletion and kidney and cardiac defects associated with VACTERL association.

Authors: Watanabe, Daisuke Nakato, Daisuke Yamada, Mamiko et al.

Source: Pediatric Nephrology. Aug2024, Vol. 39 Issue 8, p2347-2349. 3p.

A Prevalence Estimation of Exstrophy and Epispadias in Germany From Public Health Insurance Data.

Authors: Ebert AK Zwink N Reutter HM et al.

Source: Frontiers in pediatrics [Front Pediatr] 2021 Oct 26; Vol. 9, pp. 648414. Date of Electronic Publication: 2021 Oct 26 (Print Publication: 2021).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE

Clinical and pathological investigation of oligomeganephronia.

Authors: Kitakado, Hideaki Horinouchi, Tomoko Masuda, Chika et al.

Source: Pediatric Nephrology. Mar2023, Vol. 38 Issue 3, p757-762. 6p. 2 Charts, 1 Graph.

Circulating cardiovascular microRNAs in critically ill COVID‐19 patients.

Authors: Garg, Ankita Seeliger, Benjamin Derda, Anselm A. et al.

Source: European Journal of Heart Failure. Mar2021, Vol. 23 Issue 3, p468-475. 8p. 1 Diagram, 2 Charts, 3 Graphs.

Medium-long term bowel function and quality of life in complete Currarino syndrome.

Authors: Cao Y Pang W Zhang Z et al.

Source: Pediatric surgery international [Pediatr Surg Int] 2026 Jul 15; Vol. 42 (1). Date of Electronic Publication: 2026 Jul 15.

Publication Type: Journal Article

Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8609169 Publication Model: Electronic Cited Medium: Internet ISSN: 1437-9813 (Electronic) Linking ISSN: 01790358 NLM ISO Abbreviation: Pediatr Surg Int Subsets: MEDLINE

Quality of life in patients undergoing surgical correction of the exstrophy-epispadias complex in childhood.

Authors: Leite GDS Pereira LFV Venturini BA et al.

Source: World journal of urology [World J Urol] 2026 Jun 15; Vol. 44 (1). Date of Electronic Publication: 2026 Jun 15.

Publication Type: Journal Article

Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8307716 Publication Model: Electronic Cited Medium: Internet ISSN: 1433-8726 (Electronic) Linking ISSN: 07244983 NLM ISO Abbreviation: World J Urol Subsets: MEDLINE

A three generation family with VACTERL association is found to have a rare form of diamond-blackfan anaemia.

Authors: Leshchynska I Das D O'Reilly V et al.

Corporate Authors: Leshchynska I Das D O'Reilly V et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 May; Vol. 34 (5), pp. 619-629. Date of Electronic Publication: 2026 Mar 18.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Altered O‐glycosylation of β1‐adrenergic receptor N‐terminal single‐nucleotide variants modulates receptor processing and functional activity.

Authors: Tuhkanen, Hanna E. Haasiomäki, Ilona J. Lackman, Jarkko J. et al.

Source: FEBS Journal. Mar2025, Vol. 292 Issue 5, p998-1018. 21p.

Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.

Authors: Brosens E Peters NCJ van Weelden KS et al.

Source: Frontiers in pediatrics [Front Pediatr] 2022 Feb 03; Vol. 9, pp. 800915. Date of Electronic Publication: 2022 Feb 03 (Print Publication: 2021).

Publication Type: Journal Article; Review

Journal Info: Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE

A Comprehensive Review of the Complete Primary Repair Technique for Bladder-Exstrophy-Epispadias Reconstruction: First Surgical Attempt Should Be the Best One.

Authors: Torabinavid, Parham Kajbafzadeh, Abdol-Mohammad

Source: Urology Journal. Jan/Feb2025, Vol. 22 Issue 1, p1-13. 13p.

آژنزی ساکرال کیست تراتوم و ناهنجاری واژن در یک زن جوان گزارش موردی.

Alternate Title: Sacral Agenesia, Teratoma Cyst and Vaginal Abnormality in a Young Woman (Case Report).

Authors: مهدی تیوتور دکتر مهدی محمدی &#1578 محمدجواد دهقانی et al.

Source: Iranian Journal of Orthopaedic Surgery. Winter2024, Vol. 23 Issue 1, p36-38. 7p.

SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.

Authors: Bukowska-Olech, Ewelina Sowińska-Seidler, Anna Wierzba, Jolanta et al.

Source: Orphanet Journal of Rare Diseases. 8/26/2022, Vol. 17 Issue 1, p1-8. 8p.