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Ochronosis
Melanocytes and Their Diseases
University of Cincinnati
Amino Acid Disorders
Quality of Life and Photodermatoses in People with Albinism in Benin City Nigeria
Publications (1838-2000)
Alkaptonuria
Biochemical Investigations in the Rare Disease Alkaptonuria: Studies on the Metabolome and the Nature of Ochronotic Pigment
Alkaptonuria and Ochronosis – Experience from Slovakia Alkaptonúria a Ochronóza – Skúsenosti Zo Slovenska
Table I. Genodermatoses with Known Gene Defects 92 Pulkkinen
Oxidative Stress and Mechanisms of Ochronosis in Alkaptonuria
Spectrophotometric Assays for Sensing Tyrosinase Activity and Their Applications
Inherited Enzyme Defects: a Review
Ochronotic Pigmentation Is Caused by Homogentisic Acid and Is the Key Event in Alkaptonuria 2 Leading to the Destructive Consequences of the Disease – a Review
Redox Proteomics Gives Insights Into the Role of Oxidative Stress in Alkaptonuria
CLINICAL and PATHOLOGICAL FINDINGS in OCHRONOSIS 25 Urinary Bladder
Subclinical Ochronosis Features in Alkaptonuria a Cross-Sectional
Subclinical Ochronosis Features in Alkaptonuria: a Cross-Sectional Study
Long-Term Outcomes and Practical Considerations in The
Top View
21 Genodermatoses
18 Disorders of Tyrosine Metabolism
Rare Diseases: Why You Should Care George Everett MD MS Rare Diseases
Descriptions of Phenotypes
Boards' Fodder #2
Exogenous Ochronosis with Use of Low Potency Hydroquinone in a Caucasian Patient Luke Maxfield1* and David A
A Report Submitted to the Faculty of Medicine,. Oniversi Ty of The
Ochronosis and Kashin-Beck Disease In
Alkaptonuria- an Inborn Error of Amino Acid Metabolism
Effects of Ascorbic Acid in Alkaptonuria: Alterations in Benzoquinone Acetic Acid and an Ontogenic Effect in Infancy
NHGRI Abstracts
The Potential of Nitisinone for the Treatment of Alkaptonuria
Orfadin, Nitisinone
Alkaptonuria and Ochronosis International Journal of Surgery
4 Disorders of Tyrosine Degradation Elisabeth Holme
Incidentally Discovered Ochronosis Explaining Decades of Chronic Pain