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Minimum birth prevalence of mitochondrial respiratory chain disorders in children

Brain (London, England : 1878), 2003-08, Vol.126 (8), p.1905-1912

2003

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Clinical and Experimental Results on Cardiac Troponin Expression in Duchenne Muscular Dystrophy

Clinical chemistry (Baltimore, Md.), 2001-03, Vol.47 (3), p.451-458

2001

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Angeborene Störungen des Karnitinzyklus und der Fettsäuren-β-Oxidation

Kinder- und Jugendmedizin, 2004, Vol.4 (3), p.107-112

2004

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Lung function and symptom perception in children with asthma and their parents

Pediatric pulmonology, 2003-01, Vol.35 (1), p.23-28

2003

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Selektives Essverhalten und Hepatopathie bei einem 2 Jahre alten Jungen

Kinder- und Jugendmedizin, 2014, Vol.14 (4), p.240-243

2014

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The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients

Clinical pediatrics, 2003-10, Vol.42 (8), p.703-710

2003

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Yeast mediates lactic acidosis suppression after antibiotic cocktail treatment in short small bowel?

Scandinavian journal of gastroenterology, 2005-10, Vol.40 (10), p.1246-1250

2005

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Oral creatine supplementation in Duchenne muscular dystrophy: a clinical and 31P magnetic resonance spectroscopy study

Neurological research (New York), 2000-03, Vol.22 (2), p.145-150

2000

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Different clinical aspects of debrancher deficiency myopathy

Journal of Neurology, Neurosurgery and Psychiatry, 1999-09, Vol.67 (3), p.364-368

1999

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High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disorders

Molecular and cellular biochemistry, 1997-09, Vol.174 (1-2), p.71-78

1997

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Successful treatment of acute respiratory distress syndrome and severe pulmonary hypertension in a child with Bordetella pertussis infection

Wiener Klinische Wochenschrift, 2004-11, Vol.116 (21-22), p.760-762

2004

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Successful treatment of ARDS and severe pulmonary hypertension in a child with Bordetella pertussis infection

Wiener Klinische Wochenschrift, 2004-11, Vol.116 (21-22), p.760-762

2004

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Complications of percutaneous insertion of Hickman catheters in children

Journal of pediatric surgery, 1999-10, Vol.34 (10), p.1510-1513

1999

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Plasma concentrations and renal clearance of orotic acid in argininosuccinic acid synthetase deficiency

Pediatric nephrology (Berlin, West), 1999-11, Vol.13 (9), p.912-916

1999

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Update on white matter genetic disorders

Pediatric neurology, 2001-10, Vol.25 (4), p.348-348

2001

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Oral creatine supplementation in Duchenne muscular dystrophy: A clinical and 31P magnetic resonance spectroscpy study

Neurological research (New York), 2000-03, Vol.22 (2), p.145

2000

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Complications in Early Diagnosis and Treatment of Two Infants With Long‐Chain Fatty Acid β‐Oxidation Defects

Journal of pediatric gastroenterology and nutrition, 2000-10, Vol.31 (4), p.448-452

2000

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Oral creatine supplementation in Duchenne muscular dystrophy: A clinical and 31 P magnetic resonance spectroscopy study

Neurological research (New York), 2000-03, Vol.22 (2), p.145-150

2000

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Complications in Early Diagnosis and Treatment of Two Infants With Long-Chain Fatty Acid β-Oxidation Defects

Journal of pediatric gastroenterology and nutrition, 2000-10, Vol.31 (4), p.448-452

2000

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Update on white matter genetic disorders

Pediatric neurology, 2001-10, Vol.25 (4), p.347-348

2001

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Methionine loading in a Down's syndrome patient with cerebral infarction

Annals of clinical biochemistry, 1999-03, Vol.36 ( Pt 2) (2), p.252-255

1999

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Normal ascorbic acid in cerebrospinal fluid of patients with infantile neuronal ceroid-lipofuscinosis

Metabolic brain disease, 1999-03, Vol.14 (1), p.67-70

1999

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Prospective analysis of nosocomial infections in neurological intensive care patients: Prophylactic aspects and possibilities; the selective decontamination (SDD)

Skladal, Daniela

1991

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Minimum birth prevalence of mitochondrial respiratory chain disorders in children

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

Clinical and Experimental Results on Cardiac Troponin Expression in Duchenne Muscular Dystrophy

Angeborene Störungen des Karnitinzyklus und der Fettsäuren-β-Oxidation

Lung function and symptom perception in children with asthma and their parents

Selektives Essverhalten und Hepatopathie bei einem 2 Jahre alten Jungen

The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients

Yeast mediates lactic acidosis suppression after antibiotic cocktail treatment in short small bowel?

Oral creatine supplementation in Duchenne muscular dystrophy: a clinical and 31P magnetic resonance spectroscopy study

Different clinical aspects of debrancher deficiency myopathy

High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disorders

Successful treatment of acute respiratory distress syndrome and severe pulmonary hypertension in a child with Bordetella pertussis infection

Successful treatment of ARDS and severe pulmonary hypertension in a child with Bordetella pertussis infection

Complications of percutaneous insertion of Hickman catheters in children

Plasma concentrations and renal clearance of orotic acid in argininosuccinic acid synthetase deficiency

Update on white matter genetic disorders

Oral creatine supplementation in Duchenne muscular dystrophy: A clinical and 31P magnetic resonance spectroscpy study

Complications in Early Diagnosis and Treatment of Two Infants With Long‐Chain Fatty Acid β‐Oxidation Defects

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients: ASS MUTATIONS IN CITRULLINEMIA

Oral creatine supplementation in Duchenne muscular dystrophy: A clinical and 31 P magnetic resonance spectroscopy study

Complications in Early Diagnosis and Treatment of Two Infants With Long-Chain Fatty Acid β-Oxidation Defects

Update on white matter genetic disorders

Methionine loading in a Down's syndrome patient with cerebral infarction

Normal ascorbic acid in cerebrospinal fluid of patients with infantile neuronal ceroid-lipofuscinosis

Prospective analysis of nosocomial infections in neurological intensive care patients: Prophylactic aspects and possibilities; the selective decontamination (SDD)

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