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Antepartum risk factors for newborn encephalopathy: the Western Australian case-control study

BMJ (Online), 1998-12, Vol.317 (7172), p.1549

International edition, 1998

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Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia

Journal of neurology, 2015-08, Vol.262 (8), p.1822-1827

2015

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Next generation sequencing for neurological diseases: New hope or new hype?

Clinical neurology and neurosurgery, 2013-07, Vol.115 (7), p.948-953

2013

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Primary dysmenorrhea in young Western Australian women: prevalence, impact, and knowledge of treatment

Journal of adolescent health, 1999-07, Vol.25 (1), p.40-45

1999

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Voxel-based analysis in neuroferritinopathy expands the phenotype and determines radiological correlates of disease severity

Journal of neurology, 2015-10, Vol.262 (10), p.2232-2240

2015

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Simultaneous measurement of phagocytosis and respiratory burst of leukocytes in whole blood from bottlenose dolphins ( Tursiops truncatus) utilizing flow cytometry

Veterinary immunology and immunopathology, 2011-12, Vol.144 (3), p.468-475

2011

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Studies of the SIM1 gene in relation to human obesity and obesity-related traits

International Journal of Obesity, 2007-03, Vol.31 (3), p.429-434

2007

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Intrapartum risk factors for newborn encephalopathy: the Western Australian case-control study

BMJ (Online), 1998-12, Vol.317 (7172), p.1554

1998

Volltextzugriff (PDF)

Severe fibrosis in hepatitis C virus‐infected patients is associated with increased activity of the mannan‐binding lectin (MBL)/MBL‐associated serine protease 1 (MASP‐1) complex

Clinical and experimental immunology, 2007-01, Vol.147 (1), p.90-98

2007

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Exome sequencing in dementia with Lewy bodies

Translational psychiatry, 2016-02, Vol.6 (2), p.e728-e728

2016

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The CART gene and human obesity: mutational analysis and population genetics

Diabetes (New York, N.Y.), 2000-05, Vol.49 (5), p.872-875

2000

Volltextzugriff (PDF)

An unusual gait following the discovery of a new disease

Practical Neurology, 2011-04, Vol.11 (2), p.81-84

2011

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Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

The Journal of clinical investigation, 2000-07, Vol.106 (2), p.271-279

2000

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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Human molecular genetics, 2002-08, Vol.11 (17), p.1997-2004

2002

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Exome sequencing: how to understand it

Practical neurology, 2013-12, Vol.13 (6), p.399-407

2013

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Acta neuropathologica, 2019-08, Vol.138 (2), p.237-250

2019

Volltextzugriff (PDF)

Oral glutamine increases circulating glucagon-like peptide 1, glucagon, and insulin concentrations in lean, obese, and type 2 diabetic subjects

The American journal of clinical nutrition, 2009-01, Vol.89 (1), p.106-113

2009

Volltextzugriff (PDF)

Maternal awareness of fetal seizures in pregnancies resulting in newborn encephalopathy

Acta obstetricia et gynecologica Scandinavica, 2000-09, Vol.79 (9), p.787-789

2000

Volltextzugriff (PDF)

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Human molecular genetics, 2009-09, Vol.18 (17), p.3257-3265

2009

Volltextzugriff (PDF)

Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

The New England journal of medicine, 2007-01, Vol.356 (3), p.237-247

2007

Volltextzugriff (PDF)

The Sleep/Wake Cycle is Directly Modulated by Changes in Energy Balance

Sleep (New York, N.Y.), 2016-09, Vol.39 (9), p.1691-1700

2016

Volltextzugriff (PDF)

Maternal thyroid disease: a risk factor for newborn encephalopathy in term infants

BJOG : an international journal of obstetrics and gynaecology, 2000-06, Vol.107 (6), p.798-801

2000

Volltextzugriff (PDF)

Loss of Function of the Melanocortin 2 Receptor Accessory Protein 2 Is Associated with Mammalian Obesity

Science (American Association for the Advancement of Science), 2013-07, Vol.341 (6143), p.275-278

2013

Volltextzugriff (PDF)

Why is the placenta being ignored?

Australian & New Zealand journal of obstetrics & gynaecology, 2000-08, Vol.40 (3), p.343-346

2000

Volltextzugriff (PDF)

Clinical Spectrum of Obesity and Mutations in the Melanocortin 4 Receptor Gene

The New England journal of medicine, 2003-03, Vol.348 (12), p.1085-1095

2003

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Antepartum risk factors for newborn encephalopathy: the Western Australian case-control study

Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia

Next generation sequencing for neurological diseases: New hope or new hype?

Primary dysmenorrhea in young Western Australian women: prevalence, impact, and knowledge of treatment

Voxel-based analysis in neuroferritinopathy expands the phenotype and determines radiological correlates of disease severity

Simultaneous measurement of phagocytosis and respiratory burst of leukocytes in whole blood from bottlenose dolphins ( Tursiops truncatus) utilizing flow cytometry

Studies of the SIM1 gene in relation to human obesity and obesity-related traits

Intrapartum risk factors for newborn encephalopathy: the Western Australian case-control study

Severe fibrosis in hepatitis C virus‐infected patients is associated with increased activity of the mannan‐binding lectin (MBL)/MBL‐associated serine protease 1 (MASP‐1) complex

Exome sequencing in dementia with Lewy bodies

The CART gene and human obesity: mutational analysis and population genetics

An unusual gait following the discovery of a new disease

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Exome sequencing: how to understand it

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Oral glutamine increases circulating glucagon-like peptide 1, glucagon, and insulin concentrations in lean, obese, and type 2 diabetic subjects

Maternal awareness of fetal seizures in pregnancies resulting in newborn encephalopathy

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

The Sleep/Wake Cycle is Directly Modulated by Changes in Energy Balance

Maternal thyroid disease: a risk factor for newborn encephalopathy in term infants

Loss of Function of the Melanocortin 2 Receptor Accessory Protein 2 Is Associated with Mammalian Obesity

Why is the placenta being ignored?

Clinical Spectrum of Obesity and Mutations in the Melanocortin 4 Receptor Gene

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