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Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease

Gut, 2002-10, Vol.51 (4), p.475-479

2002

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Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype

Human genetics, 2009-04, Vol.125 (3), p.319-326

2009

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Monogenic and chromosomal causes of isolated speech and language impairment

Journal of Medical Genetics, 2015-11, Vol.52 (11), p.719-729

2015

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Unusual cardiac presentation of congenital cytomegalovirus infection

Ultrasound in obstetrics & gynecology, 2010-01, Vol.35 (1), p.119-120

2010

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Characterization of esophageal body and lower esophageal sphincter motor function in the very premature neonate

The Journal of pediatrics, 1999-10, Vol.135 (4), p.517-521

1999

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Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation

American journal of medical genetics. Part A, 2009-03, Vol.149A (3), p.431-436

2009

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Behavior and gastroesophageal reflux in the premature neonate

Journal of pediatric gastroenterology and nutrition, 2000, Vol.30 (1), p.18-21

2000

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Retinal detachment causing unilateral blindness in a 12-year-old girl with gyrate atrophy

Journal of inherited metabolic disease, 2009-10, Vol.32 (5), p.670-671

2009

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Clinicopathological correlations in postasphyxial organ damage: a donor organ perspective

Pediatrics (Evanston), 1997-06, Vol.99 (6), p.797

1997

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Lower esophageal sphincter position in premature infants cannot be correctly estimated with current formulas

The Journal of pediatrics, 1999-10, Vol.135 (4), p.522-525

1999

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07.04 Loeys-Dietz Syndrome (LDS): In Vitro Studies of Skin Fibroblasts Showing Differences Between Mutations in the TGFBR1 and TGFBR2 Genes

Artery research, 2008, Vol.2 (3), p.92-92

2008

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P1.01 Treatment with Dexamethasone Reverses Impared Elastogenesis and Collagenogenesis in Cultures of Fibroblasts from Patients with Loeys-Dietz Syndrome (LDS)

Artery research, 2008, Vol.2 (3), p.92-92

2008

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Characterization of anorectal pressure and the anorectal inhibitory reflex in healthy preterm and term infants

The Journal of pediatrics, 2001-08, Vol.139 (2), p.233-237

2001

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Retinal detachment causing unilateral blindness in a 12-year-old girl with gyrate atrophy: Neurological manifestations of IEM in children, dedicated to Robert Surtees

Journal of inherited metabolic disease, 2009, Vol.32 (5), p.670-671

2009

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Pyruvate dehydrogenase phosphatase 1

Human genetics, 2009-04, Vol.125 (3), p.319

2009

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Al-Gazali skeletal dysplasia constitutes the lethal end of ADAMTSL2-related disorders

EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, Vol.30 (SUPPL 1), p.41

2022

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Aplasia of Cochlear Nerves and Olfactory Bulbs in Association With S0X10 Mutation

American journal of medical genetics. Part A, 2009, Vol.149 (3), p.431-436

2009

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Impact of Automatic Palliative Care Consultation for Hospitalized Patients with Advanced Cancer (S759)

Journal of pain and symptom management, 2014-02, Vol.47 (2), p.501-502

2014

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Hemangio-Endothelioma of the Corpus Cavernosum Penis: Case Report

The Journal of urology, 1960-02, Vol.83 (2), p.160-162

1960

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Afibrinogenemia, bilirubinemia, and retained dead fetus; report of a case

American journal of clinical pathology, 1958-04, Vol.29 (4), p.367-371

1958

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"The farmer had a lung"

Virginia medical monthly, 1965-12, Vol.92 (12), p.565

Barnett, C P

1965

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ISOMETRIC EXERCISE, THE ROLE OF BRIEF MAXIMAL ISOMETRIC CONTRACTIONS IN THE DEVELOPMENT OF MUSCLE STRENGTH

Virginia medical monthly, 1964-01, Vol.91, p.1

BARNETT, C P

1964

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The mechanism of clotting as it pertains to anticoagulant treatment

Bulletin - Geisinger Medical Center, 1962-11, Vol.14, p.108

BARNETT, C P

1962

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Survival rate of patients with breast cancer in a small community

Journal of the American Medical Association, 1959-10, Vol.171, p.1180

BARNETT, C P

1959

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Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease

Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype

Monogenic and chromosomal causes of isolated speech and language impairment

Unusual cardiac presentation of congenital cytomegalovirus infection

Characterization of esophageal body and lower esophageal sphincter motor function in the very premature neonate

Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation

Behavior and gastroesophageal reflux in the premature neonate

Retinal detachment causing unilateral blindness in a 12-year-old girl with gyrate atrophy

Clinicopathological correlations in postasphyxial organ damage: a donor organ perspective

Lower esophageal sphincter position in premature infants cannot be correctly estimated with current formulas

07.04 Loeys-Dietz Syndrome (LDS): In Vitro Studies of Skin Fibroblasts Showing Differences Between Mutations in the TGFBR1 and TGFBR2 Genes

P1.01 Treatment with Dexamethasone Reverses Impared Elastogenesis and Collagenogenesis in Cultures of Fibroblasts from Patients with Loeys-Dietz Syndrome (LDS)

Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders

Characterization of anorectal pressure and the anorectal inhibitory reflex in healthy preterm and term infants

Retinal detachment causing unilateral blindness in a 12-year-old girl with gyrate atrophy: Neurological manifestations of IEM in children, dedicated to Robert Surtees

Pyruvate dehydrogenase phosphatase 1

Al-Gazali skeletal dysplasia constitutes the lethal end of ADAMTSL2-related disorders

Aplasia of Cochlear Nerves and Olfactory Bulbs in Association With S0X10 Mutation

Impact of Automatic Palliative Care Consultation for Hospitalized Patients with Advanced Cancer (S759)

Hemangio-Endothelioma of the Corpus Cavernosum Penis: Case Report

Afibrinogenemia, bilirubinemia, and retained dead fetus; report of a case

"The farmer had a lung"

ISOMETRIC EXERCISE, THE ROLE OF BRIEF MAXIMAL ISOMETRIC CONTRACTIONS IN THE DEVELOPMENT OF MUSCLE STRENGTH

The mechanism of clotting as it pertains to anticoagulant treatment

Survival rate of patients with breast cancer in a small community

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