J. Filiano

发表

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

T. Mohandas, A. Mamourian, J. Moeschler, 1999, American journal of medical genetics.

Transcatheter Closure of Patent Foramen Ovale After Presumed Paradoxical Embolism

J. Newburger, J. Lock, L. Latson, 1992, Circulation.

Potassium Permanganate Can Mark the Site of Microdialysis in Brain Sections

Gengxin Chen, R. Darnall, J. Filiano, 2000 .

Skeletal muscle mitochondrial defects in nonspecific neurologic disorders.

J. Marín-García, H. Sarnat, M. Goldenthal, 1999, Pediatric neurology.

Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

A. Perez-Atayde, J. Marín-García, M. Goldenthal, 1997, Journal of Inherited Metabolic Disease.

Infantile Onset of Hereditary Ascending Spastic Paralysis With Bulbar Involvement

T. Lerman-Sagie, J. Filiano, M. Korson, 1996, Journal of child neurology.

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

J. Rosenfeld, R. Tervo, B. Torchia, 2011, Human Genetics.

Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia

T. Maeda, Y. Matsubara, Y. Aoki, 2002, Annals of neurology.

Brainstem 3H-Nicotine Receptor Binding in the Sudden Infant Death Syndrome

H. Kinney, A. Panigrahy, L. Sleeper, 1998, Journal of neuropathology and experimental neurology.

Multiple Granular Cell Tumors in a Child with Noonan Syndrome

C. A. Storm, J. Dinulos, J. Filiano, 2010, Pediatric dermatology.

Arcuate Nucleus Hypoplasia in the Sudden Infant Death Syndrome

H. Kinney, J. Filiano, 1992, Journal of neuropathology and experimental neurology.

Medullary Serotonergic Network Deficiency in the Sudden Infant Death Syndrome: Review of a 15‐Year Study of a Single Dataset

H. Kinney, W. White, J. Filiano, 2001, Journal of neuropathology and experimental neurology.

Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations

S. Kish, Y. Furukawa, J. Filiano, 2004, Movement disorders : official journal of the Movement Disorder Society.

T. Maeda, Y. Matsubara, Y. Aoki, 2003 .

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

G. Cooper, P. Fergelot, K. Devriendt, 2020, European Journal of Human Genetics.

A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model.

H. Kinney, J J Filiano, H C Kinney, 1994, Biology of the neonate.

Decreased Serotonergic Receptor Binding in Rhombic Lip‐Derived Regions of the Medulla Oblongata in the Sudden Infant Death Syndrome

H. Kinney, A. Panigrahy, L. Sleeper, 2000, Journal of neuropathology and experimental neurology.

Characterization of Hypoxia‐Induced Ventilatory Depression in Newborn Piglets

W. M. St.-John, R. Darnall, J. Filiano, 2003, Experimental physiology.

Therapeutic plasma exchange in Streptococcus pneumoniae‐associated hemolytic uremic syndrome: A case report

M. Chobanian, N. Dunbar, M. Braga, 2012, Journal of clinical apheresis.

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

J. Rosenfeld, R. Tervo, B. Torchia, 2011, Human Genetics.

Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

H. Freeze, M. Patterson, G. Srikrishna, 2000, The Journal of clinical investigation.

Cardiomyopathy Associated With Neurologic Disorders and Mitochondrial Phenotype

J. Marín-García, M. Goldenthal, J. Filiano, 2002, Journal of Child Neurology.

Mitochondrial Dysfunction in Patients With Hypotonia, Epilepsy, Autism, and Developmental Delay: HEADD Syndrome

J. Marín-García, M. Goldenthal, J. Filiano, 2002, Journal of child neurology.

Mitochondrial DNA depletion in Leigh syndrome.

A. Mamourian, J. Marín-García, M. Goldenthal, 2002, Pediatric neurology.

Association of Chiari I malformation and Williams syndrome.

B. Pober, J. Filiano, 1995, Pediatric neurology.

Prolongation of the laryngeal chemoreflex after inhibition of the rostral ventral medulla in piglets: a role in SIDS?

J. Leiter, D. Bartlett, J C Leiter, 2003, Journal of applied physiology.

The Neuropathology of the Sudden Infant Death Syndrome. A Review

H. Kinney, J. Filiano, Ronald M. Harper, 1992, Journal of neuropathology and experimental neurology.

Brainstem research in sudden infant death syndrome.

H. Kinney, J. Filiano, 1988, Pediatrician.

The effects of a GABA(A) agonist in the rostral ventral medulla on sleep and breathing in newborn piglets.

E. Nattie, Aihua Li, R. Darnall, 2001, Sleep.

Sudden infant death syndrome and brainstem research.

H. Kinney, J. Filiano, Hannah C. Kinney, 1995, Pediatric annals.

Muscimol dialysis in the rostral ventral medulla reduced the CO(2) response in awake and sleeping piglets.

E. Nattie, Aihua Li, A K Curran, 2001, Journal of applied physiology.

Candidate cell populations for respiratory chemosensitive fields in the human infant medulla

H. Kinney, J. Filiano, John C. Choi, 1990, The Journal of comparative neurology.

Decreased Kainate Receptor Binding in the Arcuate Nucleus of the Sudden Infant Death Syndrome

H. Kinney, A. Panigrahy, L. Sleeper, 1997, Journal of neuropathology and experimental neurology.

Anatomic Relationships of the Human Arcuate Nucleus of the Medulla: A Dil‐Labeling Study

H. Kinney, J. Filiano, N. Zec, 1997, Journal of neuropathology and experimental neurology.

Congenital apnea with medullary and olivary hypoplasia: a pathologic study with computer reconstructions.

R. Sidman, H. Kinney, P. Burger, 1989, Clinical neuropathology.

Alpha2 Receptor Binding in the Medulla Oblongata in the Sudden Infant Death Syndrome

H. Kinney, A. Panigrahy, L. Sleeper, 2001, Journal of neuropathology and experimental neurology.

Opsoclonus Myoclonus after human papilloma virus vaccine in a pediatric patient.

J. Filiano, James E McCarthy, 2009, Parkinsonism & related disorders.

medullaafter muscimol dialysis in the rostroventral Enhanced baroreflex-mediated inhibition of

Daniel M. Peraza, J. Leiter, D. Bartlett, 2015 .

Tritiated-naloxone binding to brainstem opioid receptors in the sudden infant death syndrome.

H. Kinney, H. Krous, J. Filiano, 1998, Journal of the autonomic nervous system.

Neurometabolic diseases in the newborn.

J. Filiano, 2006, Clinics in perinatology.

Lesion or muscimol in the rostral ventral medulla reduces ventilatory output and the CO(2) response in decerebrate piglets.

R. Darnall, J. Filiano, A. Curran, 2000, Respiration physiology.

The development of the medullary serotonergic system in the piglet

H. Kinney, R. Belliveau, J. Filiano, 2004, Autonomic Neuroscience.

Decreased muscarinic receptor binding in the arcuate nucleus in sudden infant death syndrome

H. Kinney, L. Sleeper, J J Filiano, 1995, Science.

New England Consortium: A model for medical evaluation of expanded newborn screening with tandem mass spectrometry

M. Seashore, S. Waisbren, L. Demmer, 2001, Journal of Inherited Metabolic Disease.

movements in normo- and hypercapnia during sleep Respiratory changes associated with rapid eye

E. Nattie, Aihua Li, R. Darnall, 2015 .

Tandem mass spectrometry and newborn screening: pilot data and review.

P. Kunz, J. Filiano, Sherry Gray Bellimer, 2002, Pediatric neurology.

Mitochondrial dysfunction in skeletal muscle of children with cardiomyopathy.

A. Perez-Atayde, J. Marín-García, M. Goldenthal, 1999, Pediatrics.

Comparative anatomical assessment of the piglet as a model for the developing human medullary serotonergic system

Lynn A. Sleeper, Hannah C. Kinney, H. Kinney, 2005, Brain Research Reviews.

Developmental Changes in [3H]Lysergic Acid Diethylamide ([3H]LSD) Binding to Serotonin Receptors in the Human Brainstem

H. Kinney, A. Panigrahy, J. Filiano, 1996, Journal of neuropathology and experimental neurology.