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The London Classification of gastrointestinal neuromuscular pathology: report on behalf of the Gastro 2009 International Working Group

Gut, 2010-07, Vol.59 (7), p.882-887

2010

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A Practical Guide for the Diagnosis of Primary Enteric Nervous System Disorders

Journal of pediatric gastroenterology and nutrition, 2013-11, Vol.57 (5), p.677-686

2013

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Quantitation of cellular components of the enteric nervous system in the normal human gastrointestinal tract – report on behalf of the Gastro 2009 International Working Group

Neurogastroenterology and motility, 2011-02, Vol.23 (2), p.115-124

2011

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Childhood functional gastrointestinal disorders

Gut, 1999-09, Vol.45 (suppl 2), p.II60-ii68

1999

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Consumerism in healthcare can be detrimental to child health: lessons from children with functional abdominal pain

Archives of disease in childhood, 2005-04, Vol.90 (4), p.335-333

2005

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Eosinophilic myenteric ganglionitis is associated with functional intestinal obstruction

Gut, 2003-05, Vol.52 (5), p.752-755

2003

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Chronic intestinal pseudo-obstruction: treatment and long term follow up of 44 patients

Archives of disease in childhood, 1999-07, Vol.81 (1), p.21-27

1999

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Manganese toxicity in children receiving long-term parenteral nutrition

The Lancet (British edition), 1996-05, Vol.347 (9010), p.1218-1221

1996

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Colitis in chronic granulomatous disease

Archives of disease in childhood, 2001-02, Vol.84 (2), p.147-151

2001

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Coordinated expression of 3' Hox genes during murine embryonal gut development: An enteric Hox code

Gastroenterology (New York, N.Y. 1943), 1999-12, Vol.117 (6), p.1339-1351

1999

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Intestinal ganglioneuromatosis and multiple endocrine neoplasia type 2B: implications for treatment

Gut, 1999-07, Vol.45 (1), p.143-146

1999

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Retching and vomiting in neurologically impaired children after fundoplication: Predictive preoperative factors

Journal of pediatric surgery, 2001-09, Vol.36 (9), p.1401-1404

2001

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Systemic vasculitis : A cause of indeterminate intestinal inflammation

Journal of pediatric gastroenterology and nutrition, 2006-04, Vol.42 (4), p.405-415

2006

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Thrombosis and embolism in long-term central venous access for parenteral nutrition

The Lancet (British edition), 1994-10, Vol.344 (8929), p.1043-1045

1994

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Feeding difficulties and foregut dysmotility in Noonan’s syndrome

Archives of disease in childhood, 1999-07, Vol.81 (1), p.28-31

1999

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Irritable bowel syndrome in childhood

Gastroenterology (New York, N.Y. 1943), 2001-01, Vol.120 (1), p.287-290

Milla, Peter J.

2001

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Histological phenotypes of enteric smooth muscle disease causing functional intestinal obstruction in childhood

Histopathology, 1997-08, Vol.31 (2), p.112-122

1997

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Faecal elastase 1 concentration is a marker of duodenal enteropathy

Archives of disease in childhood, 2002-01, Vol.86 (1), p.50-53

2002

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Vomiting and Gastroesophageal Motor Activity in Children with Disorders of the Central Nervous System

Journal of pediatric gastroenterology and nutrition, 1998-01, Vol.26 (1), p.56-63

1998

Volltextzugriff (PDF)

Phytosterolemia in children with parenteral nutrition—Associated cholestatic liver disease

Gastroenterology (New York, N.Y. 1943), 1993-12, Vol.105 (6), p.1806-1813

1993

Volltextzugriff (PDF)

Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade

Archives of disease in childhood, 1996-05, Vol.74 (5), p.373-378

1996

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The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28

American journal of human genetics, 1996-04, Vol.58 (4), p.743-748

1996

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Management of Fulminating Ulcerative Colitis in Childhood with Chimeric Anti‐CD25 Antibody

Journal of pediatric gastroenterology and nutrition, 2006-02, Vol.42 (2), p.245-248

2006

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Cystic Fibrosis: Present and Future

Digestion, 1998-08, Vol.59 (5), p.579-588

Milla, P.J.

1998

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A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Nature genetics, 2000-09, Vol.26 (1), p.56-60

2000

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The London Classification of gastrointestinal neuromuscular pathology: report on behalf of the Gastro 2009 International Working Group

A Practical Guide for the Diagnosis of Primary Enteric Nervous System Disorders

Quantitation of cellular components of the enteric nervous system in the normal human gastrointestinal tract – report on behalf of the Gastro 2009 International Working Group

Childhood functional gastrointestinal disorders

Consumerism in healthcare can be detrimental to child health: lessons from children with functional abdominal pain

Eosinophilic myenteric ganglionitis is associated with functional intestinal obstruction

Chronic intestinal pseudo-obstruction: treatment and long term follow up of 44 patients

Manganese toxicity in children receiving long-term parenteral nutrition

Colitis in chronic granulomatous disease

Coordinated expression of 3' Hox genes during murine embryonal gut development: An enteric Hox code

Intestinal ganglioneuromatosis and multiple endocrine neoplasia type 2B: implications for treatment

Retching and vomiting in neurologically impaired children after fundoplication: Predictive preoperative factors

Systemic vasculitis : A cause of indeterminate intestinal inflammation

Thrombosis and embolism in long-term central venous access for parenteral nutrition

Feeding difficulties and foregut dysmotility in Noonan’s syndrome

Irritable bowel syndrome in childhood

Histological phenotypes of enteric smooth muscle disease causing functional intestinal obstruction in childhood

Faecal elastase 1 concentration is a marker of duodenal enteropathy

Vomiting and Gastroesophageal Motor Activity in Children with Disorders of the Central Nervous System

Phytosterolemia in children with parenteral nutrition—Associated cholestatic liver disease

Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade

The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28

Management of Fulminating Ulcerative Colitis in Childhood with Chimeric Anti‐CD25 Antibody

Cystic Fibrosis: Present and Future

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

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