Results 81 to 90 of about 1,752 (196)

Mikrosatellitenanalyse von Chromosom 11p mit Sequenzierung des Kandidatengens WT1 bei Neuroendokrinen Pankreastumoren [PDF]

open access: yes, 2005
Die molekularen Hintergründe bezüglich der Tumorgenese von Neuroendokrinen Pankreastumoren sind derzeit noch weitgehend ungeklärt. In mehreren Arbeiten wurde die Bedeutung einzelner Chromosomen untersucht.
Bartsch, Detlef (Prof. Dr.)   +1 more
core   +1 more source

Hypoglycemia episodes after biliopancreatic diversion for morbid obesity: clinical case presentation

open access: yesОжирение и метаболизм, 2013
Modifications of glucose metabolism are observed after bariatric surgery and are attributed to the increased release of incretins – biologically active gut peptides.

doaj   +1 more source

Estudio PET-TC con 18F-fluoro-L-DOPA combinado con el análisis genético para la optimización de la clasificación y tratamiento de un niño con hiperinsulinismo congénito grave [PDF]

open access: yes, 2009
BACKGROUND: Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycaemia in infancy. The differential diagnosis between focal and diffuse forms of CHI is of great importance when planning surgery. The aim of this article is to
Arbizu, J. (Javier)   +6 more
core  

Nesidioblastosis: hipoglucemia hiperinsulinémica persistente en la infancia

open access: yesMedisan, 2014
Se presentan 2 casos clínicos de recién nacidas que, entre otros síntomas, presentaron cifras bajas de glucemia mantenidas (menores 2,2 mmol/L), por lo que fueron evaluadas en el Servicio de Endocrinología del Hospital Provincial Pediátrico Docente ...
Kesia Granela Cortiñas   +4 more
doaj  

Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2012
With the advent of prenatal sonography, fetal overgrowth can be easily detected. Prenatal-onset overgrowth can be secondary to normal variants of familial tall stature, familial rapid maturation, diabetic macrosomia, and congenital nesidioblastosis, or ...
Chih-Ping Chen
doaj   +1 more source

Glucagon-like peptide-1 receptor imaging with [Lys^{40}(Ahx-HYNIC-^{99m}Tc/EDDA)NH_2]-exendin-4 for the detection of insulinoma [PDF]

open access: yes, 2013
PURPOSE: The objective of this article is to present a new method for the diagnosis of insulinoma with the use of [Lys(40)(Ahx-HYNIC-(99m)Tc/EDDA)NH(2)]-exendin-4.
Gilis-Januszewska, Aleksandra   +15 more
core   +1 more source

Случай врожденного гиперинсулинизма у ребенка [PDF]

open access: yes, 2010
ГИПЕРИНСУЛИНИЗ
Клишо, В. Е.   +2 more
core  

Przetrwała hipoglikemia hiperinsulinemiczna współistniejąca z nieaktywnym wyspiakiem trzustki [PDF]

open access: yes, 2015
The most common cause of hyperinsulinaemic hypoglycaemia in adult is insulinoma. Although nesidioblastosis is a rare but well-recognised disorder of persistent hypoglycaemia in infants, it is extremely rare in adults.
Blandamura, Stella   +4 more
core   +2 more sources

Nesidioblastosis en una escolar, a propósito de un caso

open access: yesCiencia y Salud, 2018
Introducción: La nesdioblastosis se define como proliferación de las células endocrinas pancreáticas, que comporta alteraciones en su distribución y diferenciación.
Rosario Almánzar   +4 more
doaj   +1 more source

Nesidioblastosis Treated Successfully by 85% Pancreatectomy

open access: yesThe Kurume Medical Journal, 2004
Nesidioblastosis is a rare disorder in pediatric surgery. It is caused by hypertrophy and hyperplasia of the islands of Langerhans, and can lead to persistent hyperinsulinemic hypoglycemia. If appropriate treatment is delayed there is a high risk of the development of cerebral palsy, impaired mental development, epilepsy or other forms of irreversible ...
Yoshiaki, Tanaka   +5 more
openaire   +3 more sources

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