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Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

Journal of medical genetics, 1998-08, Vol.35 (8), p.617-623

1998

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Hirschsprung's disease: the Australian Paediatric Surveillance Unit's experience

Pediatric surgery international, 2003-06, Vol.19 (4), p.247-250

2003

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Congenital central hypoventilation syndrome and Hirschsprung’s disease

Archives of disease in childhood, 1998-04, Vol.78 (4), p.316-322

1998

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Idiopathic slow transit constipation is rare. But delayed passage of meconium is common in the constipation clinic

Pediatric surgery international, 2007-12, Vol.23 (12), p.1153-1159

2007

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Congenital diaphragmatic hernia and interstitial deletion of chromosome 3

Journal of medical genetics, 2001-08, Vol.38 (8), p.556-558

2001

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Laparoscopically assisted percutaneous endoscopic gastrostomy

Pediatric surgery international, 1997-02, Vol.12 (2-3), p.130-131

1997

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Hirschsprung's Disease, colonic atresia, and absent hand: A new triad

Journal of pediatric surgery, 1997-09, Vol.32 (9), p.1368-1370

1997

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Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus

Annals of human genetics, 2008-03, Vol.72 (Pt 2), p.170-177

2008

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Interpretation of heart rate variability via detrended fluctuation analysis and αβ filter

Chaos (Woodbury, N.Y.), 2003-06, Vol.13 (2), p.467-475

2003

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Detrended fluctuation analysis: a suitable method for studying fetal heart rate variability?

Physiological measurement, 2004-06, Vol.25 (3), p.763

2004

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Evaluation of the NK2 Homeobox 1 Gene (NKX2‐1) as a Hirschsprung's Disease Locus  THIS ARTICLE HAS BEEN RETRACTED

Annals of human genetics, 2008-03, Vol.72 (2), p.170-177

2008

Volltextzugriff (PDF)

Interpretation of heart rate variability via detrended fluctuation analysis and alphabeta filter

Chaos (Woodbury, N.Y.), 2003-06, Vol.13 (2), p.467-475

2003

Volltextzugriff (PDF)

Laparoscopically assisted percutaneous endoscopic gastrostomy

Pediatric surgery international, 1997-02, Vol.12 (2-3), p.130

1997

Volltextzugriff (PDF)

Congenital diaphragmatic hernia and interstitial deletion of chromosome 3

Journal of medical genetics, 2001, Vol.38 (8), p.556-558

2001

Volltextzugriff (PDF)

Carbohydrate supplementation and exercise-induced changes in T-lymphocyte function

Journal of applied physiology (1985), 2003-09, Vol.95 (3), p.1216-1223

2003

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Randomized clinical trial of glutamine-supplemented versus standard parenteral nutrition in infants with surgical gastrointestinal disease

British journal of surgery, 2012-07, Vol.99 (7), p.929-938

2012

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A Dinucleotide Mutation in the Endothelin-B Receptor Gene Is Associated with Lethal White Foal Syndrome (LWFS); A Horse Variant of Hirschsprung Disease (HSCR)

Human molecular genetics, 1998-06, Vol.7 (6), p.1047-1052

1998

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Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

Hirschsprung's disease: the Australian Paediatric Surveillance Unit's experience

Congenital central hypoventilation syndrome and Hirschsprung’s disease

Idiopathic slow transit constipation is rare. But delayed passage of meconium is common in the constipation clinic

Congenital diaphragmatic hernia and interstitial deletion of chromosome 3

Laparoscopically assisted percutaneous endoscopic gastrostomy

Hirschsprung's Disease, colonic atresia, and absent hand: A new triad

Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus

Interpretation of heart rate variability via detrended fluctuation analysis and αβ filter

Detrended fluctuation analysis: a suitable method for studying fetal heart rate variability?

Evaluation of the NK2 Homeobox 1 Gene (NKX2‐1) as a Hirschsprung's Disease Locus  THIS ARTICLE HAS BEEN RETRACTED

Interpretation of heart rate variability via detrended fluctuation analysis and alphabeta filter

Laparoscopically assisted percutaneous endoscopic gastrostomy

Congenital diaphragmatic hernia and interstitial deletion of chromosome 3

Carbohydrate supplementation and exercise-induced changes in T-lymphocyte function

Randomized clinical trial of glutamine-supplemented versus standard parenteral nutrition in infants with surgical gastrointestinal disease

A Dinucleotide Mutation in the Endothelin-B Receptor Gene Is Associated with Lethal White Foal Syndrome (LWFS); A Horse Variant of Hirschsprung Disease (HSCR)

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