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Publications by H. Krude
Fatal Neonatal Respiratory Failure in an Infant With Congenital Hypothyroidism Due to Haploinsufficiency of the NKX2-1 Gene: Alteration of Pulmonary Surfactant Homeostasis
Archives of Disease in Childhood: Fetal and Neonatal Edition
Pediatrics
Gynecology
Perinatology
Obstetrics
Medicine
Child Health
Partielle Lipodystrophie Mit Verdacht Auf Autoimmunerkrankung
Arthritis und Rheuma
Related publications
Targeted Disruption of the Surfactant Protein B Gene Disrupts Surfactant Homeostasis, Causing Respiratory Failure in Newborn Mice.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene
Case Reports in Pediatrics
Genetic Causes of Congenital Hypothyroidism Due to Dyshormonogenesis
Current Opinion in Pediatrics
Child Health
Pediatrics
Perinatology
Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1
Chest
Cardiology
Critical Care
Cardiovascular Medicine
Intensive Care Medicine
Pulmonary
Respiratory Medicine
Congenital Hypothyroidism Due to Maternal Intake of Antithyroid Drugs
Efficacy of Pulmonary Surfactant Combined With High-Dose Ambroxol Hydrochloride in the Treatment of Neonatal Respiratory Distress Syndrome
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis.
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis
Haematologica
Hematology
Neonatal Respiratory Distress Due to Mumps.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
