DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Sarcosinemia
Sarcosinemia
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism Birmingham, UK, 4 – 7 September 2012
Sarcosinemia
Attachment a Rare and Expensive Disease List As of December 27, 2010 ICD-9 Age Disease Guidelines Code Group 042
Diseases Catalogue
Increased Prevalence of Hereditary Metabolic Diseases Among Native Indians in Manitoba and Northwestern Ontario
ORPHANET 3 (Phase 3)
A Patient with Nonketotic Hyperglycinemia: Biochemical Findings and Therapeutic Approaches
Whole Exome Sequencing Gene Package Metabolic Disorders, Version 5.1, 31-1-2020
Prevalence of Rare Diseases: Bibliographic Data
Endogenous Formaldehyde Is a Memory-Related Molecule in Mice and Humans
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Multiple Acyl-Coa Dehydrogenase Deficiency
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
WES Gene Package Metabolic Disorders.Xlsx
Organic Acidemias/Acidurias Precision Panel Overview
Ep 2188016 B1
Genetic Aspects of Renal Tubular Transport: Diversity and Topology of Carriers
Prevalence and Incidence of Rare Diseases: Bibilographic Data
Top View
(001-139) Includes: Diseases Generally Recogniz
Descriptions of Phenotypes
Disorders of Amino Acid Metabolism 1971
Metabolske Sykdommer V02
Supplemental Information
Ethylnitrosourea Mutagenesis (Metabolic Screening/Inborn Errors of Metabolism/Amino Acid Analysis/Gas Chromatography-Mass Spectrometry) CARY 0
Source: State: 12.06.2018 ORPHA68367 10507
Metabolomics in Laboratory Medicine for Inborn Errors of Metabolism
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
Orphanet Report Series 180 160 Collection 140 Rare Diseases
Transport and Metabolism of Sarcosine in Hypersarcosinemic and Normal Phenotypes
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
Rare and Expensive Case Management (REM) Program
Differential Diagnosis of (Inherited) Amino Acid Metabolism Or Transport Disorders
Pathway Analysis of Metabolic Activities Gabriele Sales 2018-05-21
NMR-Based Newborn Urine Screening for Optimized Detection of Inherited
Orphanet Report Series Rare Diseases Collection
Newborn Screening for Inborn Errors of Metabolism: a Systematic Review
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)