Urinary hydroxyproline and glycosaminoglycan excretion in Down's syndrome

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Journal of inherited metabolic disease·2009

Excess of malignancies in grandparents of children with malformations? Short communication.

Acta biologica Hungarica·2006

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

American journal of medical genetics·2002

Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.

Experimental and clinical immunogenetics·2002

[Centromere separation and malignancy].

Orvosi hetilap·2000

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation.

Clinical genetics·2000

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

Zeitschrift fur Kinderheilkunde·1975

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Incidence of malignant tumors in childhood (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

Zeitschrift fur Kinderheilkunde·1975

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Zeitschrift fur Kinderheilkunde·1975

FIS1 dependent peripheral fission exacerbates mitochondrial fragmentation and dysfunction in prion diseases.

Frontiers in neuroscience·2026

Lipemia retinalis secondary to pituitary neuroendocrine tumor: a case report.

Frontiers in medicine·2026

Combinatorial sequence elements fine-tune mitochondrial protein import to facilitate dual localization.

bioRxiv : the preprint server for biology·2026

BAG6-RNF115 Couples Protein Quality Control with Ribosome Assembly.

bioRxiv : the preprint server for biology·2026

Multi-omic analyses of the same sample using metabolomics, lipidomics, proteomics, phosphoproteomics, and glycoproteomics.

Chemical communications (Cambridge, England)·2026

Inhibiting Wnt/β-catenin-mTOR signaling enhances autophagy and porphyrin clearance in murine porphyrias with hepatic involvement.

Autophagy·2026

Related Experiment Videos

Urinary hydroxyproline and glycosaminoglycan excretion in Down's syndrome

Related Concept Videos

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Excess of malignancies in grandparents of children with malformations? Short communication.

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.

[Centromere separation and malignancy].

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation.

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

[Incidence of malignant tumors in childhood (author's transl)].

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

FIS1 dependent peripheral fission exacerbates mitochondrial fragmentation and dysfunction in prion diseases.

Lipemia retinalis secondary to pituitary neuroendocrine tumor: a case report.

Combinatorial sequence elements fine-tune mitochondrial protein import to facilitate dual localization.

BAG6-RNF115 Couples Protein Quality Control with Ribosome Assembly.

Multi-omic analyses of the same sample using metabolomics, lipidomics, proteomics, phosphoproteomics, and glycoproteomics.

Inhibiting Wnt/β-catenin-mTOR signaling enhances autophagy and porphyrin clearance in murine porphyrias with hepatic involvement.

Related Experiment Videos

Urinary hydroxyproline and glycosaminoglycan excretion in Down's syndrome

Related Concept Videos

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