Glycogenosis type Ib. Further evidence for a membrane disease

Familial clustering of infantile cirrhosis in Northern Germany: A clue to the etiology of idiopathic copper toxicosis.

The Journal of pediatrics·1999

Proteinuria and other renal functions in Wilson's disease.

Pediatric nephrology (Berlin, Germany)·1997

Functional comparison of PML-type and archetype strains of JC virus.

Journal of virology·1996

Late diagnosis of Wilson's disease in a case without onset of symptoms.

Acta neurologica Scandinavica·1995

The protein sequence and some intron positions are conserved between the switching gene swi10 of Schizosaccharomyces pombe and the human excision repair gene ERCC1.

Nucleic acids research·1992

Characterization of a novel enzyme, N6-acetyl-L-lysine: 2-oxoglutarate aminotransferase, which catalyses the second step of lysine catabolism in Candida maltosa.

Antonie van Leeuwenhoek·1992

Cranial pathologies in Noonan syndrome: clinical implications for pre-growth hormone neuroimaging.

European journal of pediatrics·2026

Safety and long-term outcomes of surgical intervention in pediatrics with necrotizing pneumonia: a retrospective cohort study.

European journal of pediatrics·2026

Pediatrics supratentorial intraventricular atypical teratoid/rhabdoid tumors: a case report and a systematic review of the literature.

European journal of pediatrics·2026

Lower pneumococcal IgG levels and respiratory hospitalisation in children with Down syndrome; an exploratory study.

European journal of pediatrics·2026

Treating through in pediatric patients: a single-center experience.

European journal of pediatrics·2026

Carbon footprint associated with neonatal intensive care unit admission of very preterm infants: A retrospective pilot study applying life cycle assessment.

European journal of pediatrics·2026

Serum metabolic characteristics of interstitial lung disease: a potential link between endocrine aging and gut-derived metabolites.

Frontiers in medicine·2026

ESCCA recommendations for managing measurement uncertainty in ISO 15189 accredited flow cytometry laboratories: A risk-based approach.

Cytometry. Part B, Clinical cytometry·2026

Host-guest recognition-based fluorescent probe for ultrasensitive detection of free bilirubin using β-cyclodextrin-functionalized gold nanoclusters.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2026

Correlation study of polysomnographic parameters, serological markers, and gut microbiota in patients with short-sleep insomnia: a real-world study.

Frontiers in microbiology·2026

Hypercobalaminemia in children: clinical characteristics and ınherited metabolic diagnoses in a tertiary-center cohort.

European journal of pediatrics·2026

Data-driven interpretation of mixed-culture polyhydroxyalkanoate accumulation using dual-target machine learning framework.

Bioresource technology·2026

Related Experiment Videos

Glycogenosis type Ib. Further evidence for a membrane disease

Related Concept Videos

Familial clustering of infantile cirrhosis in Northern Germany: A clue to the etiology of idiopathic copper toxicosis.

Proteinuria and other renal functions in Wilson's disease.

Functional comparison of PML-type and archetype strains of JC virus.

Late diagnosis of Wilson's disease in a case without onset of symptoms.

The protein sequence and some intron positions are conserved between the switching gene swi10 of Schizosaccharomyces pombe and the human excision repair gene ERCC1.

Characterization of a novel enzyme, N6-acetyl-L-lysine: 2-oxoglutarate aminotransferase, which catalyses the second step of lysine catabolism in Candida maltosa.

Cranial pathologies in Noonan syndrome: clinical implications for pre-growth hormone neuroimaging.

Safety and long-term outcomes of surgical intervention in pediatrics with necrotizing pneumonia: a retrospective cohort study.

Pediatrics supratentorial intraventricular atypical teratoid/rhabdoid tumors: a case report and a systematic review of the literature.

Lower pneumococcal IgG levels and respiratory hospitalisation in children with Down syndrome; an exploratory study.

Treating through in pediatric patients: a single-center experience.

Carbon footprint associated with neonatal intensive care unit admission of very preterm infants: A retrospective pilot study applying life cycle assessment.

Serum metabolic characteristics of interstitial lung disease: a potential link between endocrine aging and gut-derived metabolites.

ESCCA recommendations for managing measurement uncertainty in ISO 15189 accredited flow cytometry laboratories: A risk-based approach.

Host-guest recognition-based fluorescent probe for ultrasensitive detection of free bilirubin using β-cyclodextrin-functionalized gold nanoclusters.

Correlation study of polysomnographic parameters, serological markers, and gut microbiota in patients with short-sleep insomnia: a real-world study.

Hypercobalaminemia in children: clinical characteristics and ınherited metabolic diagnoses in a tertiary-center cohort.

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Glycogenosis type Ib. Further evidence for a membrane disease

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