{"id":512,"date":"2018-06-18T16:15:40","date_gmt":"2018-06-18T15:15:40","guid":{"rendered":"https:\/\/web22297.web16.mynet.at\/?page_id=512\/"},"modified":"2019-09-12T23:42:32","modified_gmt":"2019-09-12T22:42:32","slug":"litterature","status":"publish","type":"page","link":"https:\/\/inbornerrors.ch\/fr\/professionnels\/litterature\/","title":{"rendered":"Litt\u00e9rature"},"content":{"rendered":"<p>&nbsp;<\/p>\n<div class=\"uk-scope\">\n<ul class=\"uk-accordion uk-text-left \" uk-accordion=\"multiple: true\">\n\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Amino and organic acids-related disorder (AOA)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n<tr valign=\"top\">\n<td><strong>Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Guidelines-for-diagnosis-and-management...-cblF-cblG-cblJ-and-MTHFR-deficiency.pdf \">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n    \n<tr valign=\"top\">\n<td><strong>Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Guidelines-for-the-diagnosis-and-manage...cystathionine-beta-synthase-deficiency.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Proposed-guidelines-for-the-diagnosis-and-management-of-methylmalonic-and-propionic-acidemia.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Proposed-recommendations-for-diagnosing...taric-aciduria-type-I-second-revision.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Suggested-guidelines-for-the-diagnosis-...f-urea-cycle-disorders-first-revision.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>The complete European guidelines on phenylketonuria: diagnosis and treatment<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/The-complete-European-guidelines-on-phenylketonuria-diagnosis-and-treatment.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n    \n    \n    \n<\/tbody>\n<\/table><\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Carbohydrate, fatty acid oxidation and ketone bodies disorders (C-FAO)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n<tr valign=\"top\">\n<td><strong>International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/International-clinical-guideline-for-th...a-diagnosis-treatment-and-follow-up.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>Erna\u0308hrung bei Galaktosa\u0308mie Merkblatt fu\u0308r Jugendliche und Erwachsene<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Erna\u0308hrung-bei-Galaktosa\u0308mie-Merkblatt-fu\u0308r-Jugendliche-und-Erwachsene.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n<tr valign=\"top\">\n<td><strong>Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the Amerian College of Medical Genetics and Genomics (ACMG)<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Diagnosis-and-management-of-glycogen-storage-diseases-type-VI-and-IX-a-clinical-practice-resource-of-the-Amerian-College-of-Medical-Genetics-and-Genomics-ACMG.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n    \n\n<tr valign=\"top\">\n<td><strong>Alimentation pauvre en galactose pour enfants et adolescents jusqua\u0300 14 ans<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/12\/Alimentation-pauvre-en-galactose-pour-enfants-et-adolescents-jusqua\u0300-14-ans-final-1910.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n    \n\n<tr valign=\"top\">\n<td><strong>Galaktosearme Ernaehrung Patientenblatt Kinder<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/12\/Galaktosearme-Ernaehrung_Patientenblatt_Kinder-final-1910.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>  \n    \n    \n<tr valign=\"top\">\n<td><strong>Teneur en lactose et galactose de produits laitiers<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/12\/Teneur-en-lactose-et-galactose-de-produits-laitiers-final-1910.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr> \n    \n    \n<tr valign=\"top\">\n<td><strong>Galaktosearme Ernaehrung Galaktoseliste Milchprodukte fu\u0308r Kinder und Jugendliche bis 14<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2024\/03\/CH-Guideline-Galaktosaemie-Kinder-und-jugendliche-bis-14.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>     \n    \n    \n<\/tbody>\n<\/table>\n\n\n<p hidden>\n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p><\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Congenital disorders of glycosylation and disorders of intracellular trafficking (CDG)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n<tr valign=\"top\">\n<td><strong>International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/International-clinical-guidelines-for-the-management-of-phosphomannomutase-2-congenital-disorders-of-glycosylation-Diagnosis-treatment-and-follow-up.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n    \n    \n    \n<\/tbody>\n<\/table>\n\n\n\n<p hidden>   \n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p>\n<\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Disorder of pyruvate metabolism, krebs cycle defects, mitochondrial oxidative phosphorylationdisorders of thiamine transport and metabolism (PM-MD)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n<tr valign=\"top\">\n<td><strong>Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Diagnosis-and-management-of-mitochondrial-disease-a-consensus-statement-from-the-Mitochondrial-Medicine-Society.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n    \n    \n    \n<\/tbody>\n<\/table>\n\n\n\n<p hidden>    \n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p>\n<\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Disorders of Neuromodulators and other small molecules (NOMS)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">  \n<tbody>\n       \n<tr valign=\"top\">\n<td><strong>Lysine-restricted diet as adjunct therapy for pyridoxine-dependent epilepsy: the PDE consortium consensus recommendations<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Lysine-restricted-diet-as-adjunct-therapy-for-pyridoxine-dependent-epilepsy-the-PDE-consortium-consensus-recommendations.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>         \n    \n    \n<\/tbody>\n<\/table>    \n\n    \n\n\n<p hidden> \n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p>\n\n<\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Lysosomal storage disorders (LSD)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n    \n<tr valign=\"top\">\n<td><strong>European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experience<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/European-consensus-for-starting-and-stopping-enzyme-replacement-therapy-in-adult-patients-with-Pompe-disease-a-10-year-experience.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n\n\n    \n    \n    \n<\/tbody>\n<\/table>\n\n\n\n\n<p hidden>\n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p>\n<\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n        <li >\n\n    \n        <a href class=\"uk-accordion-title\">Peroxisomal disorders (PD)<\/a>\n\n        <div class=\"uk-accordion-content\">\n\n            \n            \n            \n                        <div class=\"uk-margin\">\n<table class=\"table1\">\n<tbody>\n    \n<tr valign=\"top\">\n<td><strong>Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines<\/strong>\nLink :    <a href=\"https:\/\/web22297.web16.mynet.at\/wp-content\/uploads\/2019\/09\/Peroxisome-biogenesis-disorders-in-the-Zellweger-spectrum-An-overview-of-current-diagnosis-clinical-manifestations-and-treatment-guidelines.pdf\">pdf<\/a>\n    <\/td>\n    <\/tr>\n    \n    \n    \n<\/tbody>\n<\/table>\n\n\n\n\n<p hidden>   \n<tr valign=\"top\">\n<td><strong>titel<\/strong>\nLink :    <a href=\"\/url\">pdf<\/a>\n    <\/td>\n    <\/tr>\n<\/p>\n<\/div>\n            \n            \n            \n            \n        <\/div>\n\n    <\/li>\n    \n<\/ul>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>&nbsp;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":362,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-512","page","type-page","status-publish","hentry","entry"],"_links":{"self":[{"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/pages\/512"}],"collection":[{"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/comments?post=512"}],"version-history":[{"count":4,"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/pages\/512\/revisions"}],"predecessor-version":[{"id":1315,"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/pages\/512\/revisions\/1315"}],"up":[{"embeddable":true,"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/pages\/362"}],"wp:attachment":[{"href":"https:\/\/inbornerrors.ch\/fr\/wp-json\/wp\/v2\/media?parent=512"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}