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Fanconi syndrome
Transient Acquired Fanconi Syndrome with Unusual and Rare Aetiologies: a Case Study of Two Dogs
Amino Acids (Urine)
Disease Name Tyrosinemia Type III
ACVIM Giger Cyst+Fanconi 2014F
Adult Complications of Nephropathic Cystinosis: a Systematic Review
Molecular Patterns Behind Immunological and Metabolic Alterations in Lysinuric Protein Intolerance
Non-Cystinotic Fanconi Syndrome
Lowe Syndrome: Report of a Case and Brief Literature Review
Lowe Syndrome
Renal Tubular Disorders
Lowe Syndrome
Inborn Errors of Metabolism As a Cause of Neurological Disease in Adults: an Approach to Investigation
The Generalized Aminoaciduria Seen in Patients with Hepatocyte Nuclear Factor-1 Mutations Is a Feature of All Patients with Diab
Tyrosinemia Type 1 – a Case Report FAHMIDA ISLAM1, WAHIDUZZAMAN MAZUMDER2, A.S.M
1 a Clinical Approach to Inherited Metabolic Diseases
Ocular Manifestations of Inherited Diseases Maya Eibschitz-Tsimhoni
When Low Bone Mineral Density and Fractures Is Not Osteoporosis
Hyperamino-Aciduria in Lignac-Fanconi Disease, in Galactosaemia and in an Obscure Syndrome by H
Top View
Approach to Renal Tubular Disorders
A Case of Fanconi Syndrome with Lysinuric Protein Intolerance
Liver Dysfunction in Children Cause by Metabolic Diseases: Review of 9 Cases
Newborn Screening ○○○○○○○○○○○○○○○○○○○○○○○○○
Recent Advances in Ophthalmic Genetics Genetic Counselling
The Renal Fanconi Syndrome in Cystinosis: Pathogenic Insights and Therapeutic Perspectives
Amino Acid Transport Defects in Human Inherited Metabolic Disorders
The Nephropathy of Type I Tyrosinemia After Liver Transplantation
The Oculocerebrorenal Syndrome of Lowe: an Update
Fanconi Syndrome Are on the Rise in Parts (Jamieson and Chandler, 2001)
Cystinuria: Mechanisms and Management
Inherited Disorders of Amino Acid Transport in Relation to the Kidney BRUCE A
End-Stage Renal Failure in Lowe Syndrome
Inborn Errors of Metabolism in Infancy and Early Childhood: an Update TALKAD S
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
Aminoaciduria Caused by Fanconi Syndrome in a Heifer N
Update on Lysinuric Protein Intolerance, a Multi-Faceted Disease
Abnormalities of Carbohydrate Metabolism in Idiopathic Fanconi Syndrome
Neutropenia Associated with Proximal Renal Tubular Dysfunction and Mild Bilateral Cataract
The Kidney Involvement in Inborn Errors of Metabolism Athanasios Evangeliou, Maria Gogou, Despoina Tramma
Renal Fanconi Syndrome with Ultrastructural Defects in Lysinuric Protein Intolerance Benninga, M A; Lilien, M; De Koning, T
Aminoaciduria and Glycosuria in Children
Inborn Errors of Metabolism
Metabolic Disorders in Pediatric Neurology
An Uncommon Clinical Case with Fanconi Syndrome, Acanthosis Nigricans and Hyperinsulinemia
A Mouse Model of Renal Tubular Injury of Tyrosinemia Type 1
Prevalence and Incidence of Rare Diseases
Idiopathic Fanconi Syndrome in a Family. Part I. Clinical
Late Diagnosis of Fanconi-Bickel Syndrome: ª the Author(S) 2016 DOI: 10.1177/2326409816679430 Challenges with the Diagnosis Iem.Sagepub.Com and Literature Review
Cystine Dimethylester Model of Cystinosis: Still Reliable?
Lysine Intolerance in a Variant Form of Citrullinemia
Renal Tubular Disorders
The Renal Handling of Carnitine in Patients with Selective Tubulopathy and with Fanconi Syndrome
The Fanconi Syndrome and Mechanisms of Tubular Transport Dysfunction KARL S
List of Nephropathy Genes