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Publications by G H Deutsch

Novel NKX2.1 Mutation Associated With Hypothyroidism and Lethal Respiratory Failure in a Full-Term Neonate

Journal of Perinatology

English

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Case Report of Lethal Perinatal Hypophosphatasia With Seizure and Respiratory Failure Diagnosed by ALPL Gene Mutation

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A Neonate With MuSK Congenital Myasthenic Syndrome Presenting With Refractory Respiratory Failure

Frontiers in Pediatrics

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A Novel COL4A1 Mutation in a Neonate With Intrauterine Intraventricular Hemorrhage and Porencephaly

Neonatal Medicine

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Novel Mutation and Severe Respiratory Failure in Congenital Disorders of Glycosylation Type Ix

Turkish Journal of Pediatrics

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Acute Respiratory Failure Associated With Vaping

Cardiovascular Medicine

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Ethylmalonic Encephalopathy Associated With Respiratory Failure

Eastern Journal of Medicine

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Acute Respiratory Alkalosis Associated With Low Minute Ventilation in a Patient With Severe Hypothyroidism

Canadian Journal of Anaesthesia

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A Novel Gene, FAM11A, Associated With the FRAXF CpG Island Is Transcriptionally Silent in FRAXF Full Mutation

European Journal of Human Genetics

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Two Siblings With Congenital Central Hypothyroidism Caused by a Novel Mutation in the IGSF1 Gene

Clinical Pediatric Endocrinology

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