Study objectives: To conduct screening of alkaline phosphatase (ALP) levels; compare the frequency of detection of low ALP levels using different diagnostic systems; evaluate the possibility of introducing a single «cut-off point». Materials and methods: We analyzed 5472 ALP tests were from 01.08.2013 to 30.04.2017 (672 tests been done with diagnostic system Synchron (Beckman Coulter), 4800 tests been done with system ADVIA 1800 (Siemens Vista)). Results: Identified 67 (1.2%) tests (55 patients) with low values of ALP: among them 35 patients been treated with glucocorticoids; 4 with cytostatics; the rest patients without therapy (6 were in the debut of juvenile rheumatoid arthritis (3), acute leukemia (1), Kawasaki syndrome (1), erythema no...
Hypophosphatasia (HPP) is a genetic disease caused by one or several mutations in ALPL gene encodin...
BECAUSE OF THE INCREASED interest in serum alkaline phosphatase in recent years (1-4) and the ever-i...
Hypophosphatasia (HPP) is an inborn error of metabolism characterized by low levels of serum alkalin...
Objectives: Low activity of serum alkaline phosphatase (ALP) is a hallmark of hypophosphatasia (HPP)...
Abstract Background Tissue-nonspecific alkaline phosphatase (TNSALP) encoded by the ALPL gene is of ...
[Background]: Low serum levels of alkaline phosphatase (ALP) are a hallmark of hypophosphatasia. How...
Background: Hypophosphatasia (HPP) is an inborn disease caused by pathogenic variants in ALPL. Low l...
ABSTRACT Introduction: Interpreting laboratory tests requires reference intervals (RI) that may var...
Hypophosphatasie (HPP) ist eine seltene genetische Erkrankung mit einem breiten Spektrum an biochemi...
Hypophosphatasia (HPP) is a rare and underdiagnosed condition characterized by deficient bone and te...
Background: Low serum alkaline phosphatase levels are the hallmark of hypophosphatasia, a disorder d...
Hypophosphatasia (HPP) is a rare genetic disorder characterized by low serum alkaline phosphatase (A...
Purpose: This study assesses the usefulness of alkaline phosphatase (ALP) in predicting the radiolog...
To determine if alkaline phosphatase (AP) levels are a useful screening test for rickets, the author...
Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by deficient tissue non‐specif...
Hypophosphatasia (HPP) is a genetic disease caused by one or several mutations in ALPL gene encodin...
BECAUSE OF THE INCREASED interest in serum alkaline phosphatase in recent years (1-4) and the ever-i...
Hypophosphatasia (HPP) is an inborn error of metabolism characterized by low levels of serum alkalin...
Objectives: Low activity of serum alkaline phosphatase (ALP) is a hallmark of hypophosphatasia (HPP)...
Abstract Background Tissue-nonspecific alkaline phosphatase (TNSALP) encoded by the ALPL gene is of ...
[Background]: Low serum levels of alkaline phosphatase (ALP) are a hallmark of hypophosphatasia. How...
Background: Hypophosphatasia (HPP) is an inborn disease caused by pathogenic variants in ALPL. Low l...
ABSTRACT Introduction: Interpreting laboratory tests requires reference intervals (RI) that may var...
Hypophosphatasie (HPP) ist eine seltene genetische Erkrankung mit einem breiten Spektrum an biochemi...
Hypophosphatasia (HPP) is a rare and underdiagnosed condition characterized by deficient bone and te...
Background: Low serum alkaline phosphatase levels are the hallmark of hypophosphatasia, a disorder d...
Hypophosphatasia (HPP) is a rare genetic disorder characterized by low serum alkaline phosphatase (A...
Purpose: This study assesses the usefulness of alkaline phosphatase (ALP) in predicting the radiolog...
To determine if alkaline phosphatase (AP) levels are a useful screening test for rickets, the author...
Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by deficient tissue non‐specif...
Hypophosphatasia (HPP) is a genetic disease caused by one or several mutations in ALPL gene encodin...
BECAUSE OF THE INCREASED interest in serum alkaline phosphatase in recent years (1-4) and the ever-i...
Hypophosphatasia (HPP) is an inborn error of metabolism characterized by low levels of serum alkalin...