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(Mal)nutrition in critical illness and beyond: a narrative review

Anaesthesia, 2023-06, Vol.78 (6), p.770-778

2023

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Structural properties of sodium-rich carbonate-silicate melts: An in-situ high-pressure EXAFS study on Y and Sr

Journal of physics. Conference series, 2016, Vol.712 (1), p.12083

2016

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A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa

Neurology, 2005-06, Vol.64 (11), p.1952-1954

2005

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Clinical features of pediatric Graves’ orbitopathy

International ophthalmology, 2010-12, Vol.30 (6), p.717-721

2010

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Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations

Experimental and clinical endocrinology & diabetes, 2013-06, Vol.121 (6), p.343-346

2013

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In situ characterization of liquid network structures at high pressure and temperature using X-ray absorption spectroscopy coupled with the Paris-Edinburgh press

High pressure research, 2016-07, Vol.36 (3), p.332-347

2016

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1833 Acute Necrotizing Encephalopathy of Childhood Associated with Influenza A

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A518-A519

2012

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Clinical and metabolic findings in a 6-year-old boy with a Leydig cell tumour

Acta Paediatrica, 2011-12, Vol.100 (12), p.e280-e282

2011

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Shiga-Toxigenic Escherichia coli-Inoculated Neonatal Piglets Develop Kidney Lesions That Are Comparable to Those in Humans with Hemolytic-Uremic Syndrome

Infection and Immunity, 2005, Vol.73 (1), p.612-616

2005

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Wachstumsstörungen

Monatsschrift Kinderheilkunde, 2014, Vol.162 (4), p.298-298

2014

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Uptake of colostral leukocytes in the intestinal tract of newborn calves

Veterinary immunology and immunopathology, 2002-02, Vol.85 (1), p.33-40

2002

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Genotype-Phenotype Correlations in Pompe Disease

Clinical therapeutics, 2011-06, Vol.33 (6), p.S39-S39

2011

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A Novel homozygous mutation in the solute carrier family 26 member 7 gene causes thyroid dyshormonogenesis in a girl with congenital hypothyroidism

Yearbook of Paediatric Endocrinology, 2021-09

2021

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Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V)

Experimental and clinical endocrinology & diabetes, 2005-12, Vol.113 (10), p.582-585

2005

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Monocarboxylattransporter-8-Defekt: Ursache einer muskulären Hypotonie beim Jungen

Monatsschrift Kinderheilkunde, 2016-02, Vol.164 (2), p.129-131

2016

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Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site

The Journal of clinical investigation, 1998-03, Vol.101 (5), p.1028-1035

1998

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Saccharomyces boulardii and bacillus cereus var. Toyoi influence the morphology and the mucins of the intestine of pigs

Zeitschrift für Gastroenterologie, 2002-05, Vol.40 (5), p.277-284

2002

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Morphological and immunohistochemical characterization of spontaneous mammary tumours in European hedgehogs (Erinaceus europaeus)

Journal of comparative pathology, 2007-07, Vol.137 (1), p.22-29

2007

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Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria

Animal genetics, 2005-08, Vol.36 (4), p.297-302

2005

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Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters

The journal of clinical endocrinology and metabolism, 2000-07, Vol.85 (7), p.2366-2369

2000

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Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literature

Experimental and clinical endocrinology & diabetes, 2006-05, Vol.114 (5), p.227-234

2006

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Structural controls of CO2 on Y, La and Sr incorporation in sodium-rich silicate - carbonate melts by in-situ high P-T EXAFS

Chemical geology, 2018-05, Vol.486, p.1-15

2018

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Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene

Journal of Pediatric Endocrinology and Metabolism, 2008-11, Vol.21 (11), p.1093-1098

2008

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Incidence of BVDV1 and BVDV2 Infections in Cattle Submitted for Necropsy in Northern Germany

Journal of veterinary medicine. Series B, 2006-10, Vol.53 (8), p.363-369

2006

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Wound Healing Is Not Impaired in Rats Undergoing Perioperative Treatment with the Antineoplastic Agent Taurolidine

European surgical research, 2009-01, Vol.42 (2), p.91-96

2009

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(Mal)nutrition in critical illness and beyond: a narrative review

Structural properties of sodium-rich carbonate-silicate melts: An in-situ high-pressure EXAFS study on Y and Sr

A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa

Clinical features of pediatric Graves’ orbitopathy

Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations

In situ characterization of liquid network structures at high pressure and temperature using X-ray absorption spectroscopy coupled with the Paris-Edinburgh press

1833 Acute Necrotizing Encephalopathy of Childhood Associated with Influenza A

Clinical and metabolic findings in a 6-year-old boy with a Leydig cell tumour

Shiga-Toxigenic Escherichia coli-Inoculated Neonatal Piglets Develop Kidney Lesions That Are Comparable to Those in Humans with Hemolytic-Uremic Syndrome

Wachstumsstörungen

Uptake of colostral leukocytes in the intestinal tract of newborn calves

Genotype-Phenotype Correlations in Pompe Disease

A Novel homozygous mutation in the solute carrier family 26 member 7 gene causes thyroid dyshormonogenesis in a girl with congenital hypothyroidism

Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V)

Monocarboxylattransporter-8-Defekt: Ursache einer muskulären Hypotonie beim Jungen

Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site

Saccharomyces boulardii and bacillus cereus var. Toyoi influence the morphology and the mucins of the intestine of pigs

Morphological and immunohistochemical characterization of spontaneous mammary tumours in European hedgehogs (Erinaceus europaeus)

Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria

Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters

Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literature

Structural controls of CO2 on Y, La and Sr incorporation in sodium-rich silicate - carbonate melts by in-situ high P-T EXAFS

Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene

Incidence of BVDV1 and BVDV2 Infections in Cattle Submitted for Necropsy in Northern Germany

Wound Healing Is Not Impaired in Rats Undergoing Perioperative Treatment with the Antineoplastic Agent Taurolidine

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