Professor of Pathology, Boston Children's Hospital

Pathology

Doctor Hannah C. Kinney, MD practices Pathology. He studied medicine at Case Western Reserve University School of Medicine. Hannah Kinney is a published MD. He published 100 publications, including: '3-Dimensional anatomic relationship of serotonergic and muscarinic receptor binding in the pontine reticular formation of the human infant brainstem.'

Publications

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• Hippocampal malformation associated with sudden death in early childhood: a neuropathologic study : Part 2 of the investigations of The San Diego SUDC Research Project.
• The Structural Connectome of the Human Central Homeostatic Network.
• Dentate gyrus abnormalities in sudden unexplained death in infants: morphological marker of underlying brain vulnerability.
• Prenatal Nicotine Exposure Selectively Affects Nicotinic Receptor Expression in Primary and Associative Visual Cortices of The Fetal Baboon.
• Serotonin metabolites in the cerebrospinal fluid in sudden infant death syndrome.
• Neuropathologic studies of the encephalopathy of prematurity in the late preterm infant.
• Potential Asphyxia and Brainstem Abnormalities in Sudden and Unexpected Death in Infants.
• Witnessed sleep-related seizure and sudden unexpected death in infancy: a case report.
• Disconnection of the Ascending Arousal System in Traumatic Coma.
• The Human Connectome Project and Beyond: Initial Applications of 300 mT/m Gradients.
• Development of Brainstem 5-HT1A Receptor Binding Sites in Serotonin-Deficient Mice.
• Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
• Caffeine improves the ability of serotonin-deficient (Pet-1-/-) mice to survive episodic asphyxia.
• Sudden and unexpected death in early life: proceedings of a symposium in honor of Dr. Henry F. Krous.
• Expression of EAAT2 in neurons and protoplasmic astrocytes during human cortical development.
• Radial Coherence of Diffusion Tractography in the Cerebral White Matter of the Human Fetus: Neuroanatomic Insights.
• Modeling the encephalopathy of prematurity in animals: the important role of translational research.
• Neuroanatomic Connectivity of the Human Ascending Arousal System Critical to Consciousness and Its Disorders.
• Inheritance of febrile seizures in sudden unexplained death in toddlers.
• Brainstem deficiency of the 14-3-3 regulator of serotonin synthesis: a proteomics analysis in the sudden infant death syndrome.
• Late development of the GABAergic system in the human cerebral cortex and white matter.
• Decreased GABAA Receptor Binding in the Medullary Serotonergic System in the Sudden Infant Death Syndrome.
• Reprint of "The developing oligodendrocyte: key cellular target in brain injury in the premature infant"
• Failed heart rate recovery at a critical age in 5-HT-deficient mice exposed to episodic anoxia: Implications for SIDS.
• The serotonergic anatomy of the developing human medulla oblongata: Implications for pediatric disorders of homeostasis.
• Aberrant Upregulation of Astroglial Ceramide Potentiates Oligodendrocyte Injury.
• Maternal dietary tryptophan deficiency alters cardiorespiratory control in rat pups.
• Potential neuronal repair in cerebral white matter injury in the human neonate.
• Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego Dataset.
• Brainstem serotonergic deficiency in sudden infant death syndrome.
• A practical classification schema incorporating consideration of possible asphyxia in cases of sudden unexpected infant death.
• Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.
• The encephalopathy of prematurity: one pediatric neuropathologist's perspective.
• Sudden death, febrile seizures, and hippocampal and temporal lobe maldevelopment in toddlers: a new entity.
• Prenatal nicotine-exposure alters fetal autonomic activity and medullary neurotransmitter receptors: implications for sudden infant death syndrome.
• The sudden infant death syndrome.
• Thalamic damage in periventricular leukomalacia: novel pathologic observations relevant to cognitive deficits in survivors of prematurity.
• Brainstem mechanisms underlying the sudden infant death syndrome: evidence from human pathologic studies.
• The brainstem and serotonin in the sudden infant death syndrome.
• Structural abnormalities in the brainstem and cerebellum in congenital central hypoventilation syndrome: commentary on the article by Kumar et al. on page 275.
• Diffuse axonal injury in periventricular leukomalacia as determined by apoptotic marker fractin.
• Glutamate transporter EAAT2 expression is up-regulated in reactive astrocytes in human periventricular leukomalacia.
• Fetal mechanisms in neurodevelopmental disorders.
• Sudden death in toddlers with viral meningitis, massive cerebral edema, and neurogenic pulmonary edema and hemorrhage: report of two cases.
• Sudden death in toddlers associated with developmental abnormalities of the hippocampus: a report of five cases.
• The glutamate transporter EAAT2 is transiently expressed in developing human cerebral white matter.
• Sudden unexpected death in childhood associated with cardiac rhabdomyoma, involuting adrenal ganglioneuroma, and megalencephaly: another expression of tuberous sclerosis?
• The late preterm infant and the control of breathing, sleep, and brainstem development: a review.
• Is the late preterm infant more vulnerable to gray matter injury than the term infant?
• Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.
• Lipid peroxidation during human cerebral myelination.
• Development of microglia in the cerebral white matter of the human fetus and infant.
• Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.
• The near-term (late preterm) human brain and risk for periventricular leukomalacia: a review.
• Serotonin transporter abnormality in the dorsal motor nucleus of the vagus in Rett syndrome: potential implications for clinical autonomic dysfunction.
• Abnormalities of the brainstem serotonergic system in the sudden infant death syndrome: a review.
• Subtle autonomic and respiratory dysfunction in sudden infant death syndrome associated with serotonergic brainstem abnormalities: a case report.
• Mechanism of JCV entry into oligodendrocytes.
• Sudden Infant Death Syndrome: increased carotid-body dopamine and noradrenaline content.
• Axonal development in the cerebral white matter of the human fetus and infant.
• Chronic fluoxetine microdialysis into the medullary raphe nuclei of the rat, but not systemic administration, increases the ventilatory response to CO2.
• Developmental lag in superoxide dismutases relative to other antioxidant enzymes in premyelinated human telencephalic white matter.
• Differential development of 5-HT receptor and the serotonin transporter binding in the human infant medulla.
• Serotonergic brainstem abnormalities in Northern Plains Indians with the sudden infant death syndrome.
• Nitrosative and oxidative injury to premyelinating oligodendrocytes in periventricular leukomalacia.
• Risk factors for sudden infant death syndrome among northern plains Indians.
• Arrested oligodendrocyte lineage progression during human cerebral white matter development: dissociation between the timing of progenitor differentiation and myelinog...
• Neuropathology associated with stillbirth.
• Nicotine, serotonin, and sudden infant death syndrome.
• The fetal alcohol syndrome and neuroblastoma.
• Subacute diencephalic angioencephalopathy--report of an additional case.
• Abnormal microstructure of the atrophic thalamus in preterm survivors with periventricular leukomalacia.
• Ventilatory response to hypercapnia and hypoxia after extensive lesion of medullary serotonergic neurons in newborn conscious piglets.
• Oxidative and nitrative injury in periventricular leukomalacia: a review.
• Volumetric brain differences in children with periventricular T2-signal hyperintensities: a grouping by gestational age at birth.
• Anatomic relationships of the human nucleus paragigantocellularis lateralis: a DiI labeling study.
• Distribution of alpha 2-adrenergic receptor binding in the developing human brain stem.
• Alpha2 receptor binding in the medulla oblongata in the sudden infant death syndrome.
• Medullary serotonergic network deficiency in the sudden infant death syndrome: review of a 15-year study of a single dataset.
• Late oligodendrocyte progenitors coincide with the developmental window of vulnerability for human perinatal white matter injury.
• Differential expression of glutamate receptor subtypes in human brainstem sites involved in perinatal hypoxia-ischemia.
• Decreased serotonergic receptor binding in rhombic lip-derived regions of the medulla oblongata in the sudden infant death syndrome.
• Sleep influences on homeostatic functions: implications for sudden infant death syndrome.
• Early developmental changes in the chemoarchitecture of the human inferior olive: a review.
• 3-Dimensional anatomic relationship of serotonergic and muscarinic receptor binding in the pontine reticular formation of the human infant brainstem.
• Brainstem 3H-nicotine receptor binding in the sudden infant death syndrome.
• Human oligodendroglial development: relationship to periventricular leukomalacia.
• Tritiated-naloxone binding to brainstem opioid receptors in the sudden infant death syndrome.
• Developmental changes in heterogeneous patterns of neurotransmitter receptor binding in the human interpeduncular nucleus.
• Decreased kainate receptor binding in the arcuate nucleus of the sudden infant death syndrome.
• Anatomic relationships of the human arcuate nucleus of the medulla: a DiI-labeling study.
• Expression of the homeobox-containing genes EN1 and EN2 in human fetal midgestational medulla and cerebellum.
• Brainstem tegmental necrosis and olivary hypoplasia: a lethal entity associated with congenital apnea.
• Reciprocal entorhinal-hippocampal connections established by human fetal midgestation.
• Developmental changes in neurotransmitter receptor binding in the human periaqueductal gray.
• Massive opioid resistance in an infant with a localized metastasis to the midbrain periaqueductal gray.
• Three-dimensional distribution of [3H]quinuclidinyl benzilate binding to muscarinic cholinergic receptors in the developing human brainstem.
• Developmental changes in [3H]lysergic acid diethylamide ([3H]LSD) binding to serotonin receptors in the human brainstem.
• Anatomic distribution of the growth-associated protein GAP-43 in the developing human brainstem.

Schools

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• Case Western Reserve University School of Medicine

• Childrens Hospital Boston

• Childrens Hospital Of Philapa

• Duke University Med Center Nc

• Harvard Med School

Doctors Specialties

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• Neuropathology
• Pathology

Accepted Insurances

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• First Health (Coventry Health Care) PPO

Education

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• Boston Children's Hospital
• Duke University Hospital
• Children's Hospital of Philadelphia
• Case Western Reserve University School of Medicine

Hospital

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• Boston Children's Hospital

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