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Nagoud Schukfeh

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Articles 34
Citations 168
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Recent Articles
1.
Garrisi E, Muller C, Ure B, Carlens J, Dingemann J, Schukfeh N
Eur J Pediatr Surg . 2024 Oct; 35(1):52-59. PMID: 39419066
Background/purpose:  Gastroesophageal reflux disease (GERD) after lung transplantation (LuTx) can lead to chronic lung allograft dysfunction. Our aim was to assess the prevalence of GERD in pediatric LuTx recipients and...
2.
Schukfeh N, Sivaraman K, Schmidt A, Vieten G, Dingemann J, Weidner J, et al.
Pediatr Surg Int . 2024 Sep; 40(1):258. PMID: 39347946
Purpose: Intestinal anastomosis is a routine procedure in pediatric surgery, with leakage being a significant complication. Human alpha1-antitrypsin (AAT), whose physiological serum concentrations range from 0.9-2.0 mg/ml, is known to...
3.
Pardey N, Zeidler J, Blaser J, Becker N, Dingemann J, Ure B, et al.
Eur J Pediatr Surg . 2024 Sep; 35(1):43-51. PMID: 39322202
Background:  Esophageal atresia (EA) is a rare disease requiring surgical repair, usually within the first days of life. Patients with EA require intensive postoperative care and often have comorbidities. There...
4.
Abo-Namous R, Kuebler J, Potthoff A, Madadi-Sanjani O, Uecker M, Dingemann J, et al.
Innov Surg Sci . 2024 Aug; 9(2):93-98. PMID: 39100717
Objectives: Choledochal malformation (CM) is a rare disease that can lead to malignancy and potential long-term sequelae despite surgical resection. There is no long-term follow-up data on patients after CM...
5.
Lof Granstrom A, Irvine W, Telle Hoel A, Tabbers M, Kyrklund K, Fascetti-Leon F, et al.
J Pediatr Surg . 2024 May; 59(10):161565. PMID: 38763854
Background: Hirschsprung disease is a congenital intestinal motility disorder characterized by an absence of enteric ganglion cells. Total colonic aganglionosis and near total or total intestinal aganglionosis, defined as absence...
6.
Pfister E, Jaeger V, Karch A, Shay D, Schukfeh N, Ohlendorf J, et al.
Hepatol Commun . 2023 Mar; 7(4). PMID: 36995996
Background: Bile salt export pump (ABCB11) deficiency [Progressive familial intrahepatic cholestasis (PFIC2)] is the most common genetic cause of PFIC and is associated with pruritus and progressive liver disease. Surgical...
7.
Schukfeh N, Liu B, DeLuca D, Tumpara S, Nikolin C, Immenschuh S, et al.
Eur J Immunol . 2022 Nov; 53(1):e2250019. PMID: 36321537
Nowadays laparoscopic interventions enable the collection of resident macrophage populations out of the human cavities. We employed this technique to isolate pleural monocytes/macrophages from healthy young adults who underwent a...
8.
Kiblawi R, Beck C, Keil O, Schukfeh N, Hofmann A, Ure B, et al.
Eur J Pediatr Surg . 2022 Oct; 33(1):26-34. PMID: 36220133
Introduction:  Minimally invasive surgery (i.e., laparoscopy) and minimally invasive anesthesia (i.e., caudal anesthesia with spontaneous respiration) have separately shown benefits for inguinal hernia repair in infants, yet to what degree...
9.
Schukfeh N, Abo-Namous R, Madadi-Sanjani O, Uecker M, Petersen C, Ure B, et al.
Eur J Pediatr Surg . 2022 Jun; 32(6):521-528. PMID: 35764302
Background:  Numerous studies from Asian countries, including large collectives, have reported excellent results after laparoscopic resection of choledochal malformation (CM). However, the role of laparoscopic CM resection is still controversial...
10.
Hulscher J, Kuebler J, Bruggink J, Davenport M, Scholz S, Petersen C, et al.
J Clin Med . 2022 Feb; 11(4). PMID: 35207421
Background: While congenital choledochal malformation (CCM) is relatively well known within the pediatric surgical and pediatric gastroenterological communities, many controversies and questions remain. Methods: In this paper, we will discuss...