Jin S. Hahn, MD

Pediatric neurologist, Neurophysiologist

Professor of Neurology, of Pediatrics and, by courtesy, of Neurosurgery at the Stanford University Medical Center

Comprehensive Epilepsy Program

  • 300 Pasteur Drive
  • Stanford, CA 94305
  • Phone: 650-723-6469
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Professional Education

Board Certification, American Board of Psychiatry and Neurology, Clinical Neurophysiology (1992)

Board Certification, American Board of Preventive Medicine, Clinical Informatics (2013)

Residency: Children's Hospital Boston (1987) MA

Residency: Children's Hospital Boston (1984) MA

Fellowship: Stanford University School of Medicine (1989) CA

Medical Education: Harvard Medical School (1982) MA

Internship: Children's Hospital Boston (1983) MA

Board Certification: Neurology - Child Neurology, American Board of Psychiatry and Neurology (1989)

Board Certification: Pediatrics, American Board of Pediatrics (1987)

MD, Harvard Medical School, Medicine (1982)

Fellowship, Stanford Biomedical Informatics, Clinical Informatics (1999)

Administrative Appointments

Medical Director of Clinical Informatics, Lucile Packard Children's Hospital (2012 - Present)

Chief Medical Information Officer, Lucile Packard Children's Hospital (2004 - 2008)

Division Chief, Pediatric Neurology, Stanford Dept. of Neurology (1996 - 2008)

Executive Committee, Stanford Center for Clinical Informatics (SCCI) (2004 - 2008)

Co-director, NSADA (Neurologic Sciences Academic Development Award) Stanford (2004 - 2008)

Director of Child Neurology Residency Training Program, Dept. of Neurology & Neurological Sciences (1991 - 2008)

Service Chief, Neurology, Lucile Packard Children's Hospital (1991 - 2005)

Counselor from West, Professors of Child Neurology (2004 - 2006)

Chairman of CNS Electronic Communications Committee, Child Neurology Society (1999 - 2005)

Agenesis of Corpus Callosum and Associated Malformations: From Aicardi to Zellweger Syndromes
Hahn JS, MacLean J, & Yeom K. (2012). Agenesis of Corpus Callosum and Associated Malformations: From Aicardi to Zellweger Syndromes. NeoReviews, 13(4).

Rapid Implementation of Inpatient Electronic Physician Documentation at an Academic Hospital
Hahn JS, Bernstein JA, McKenzie RB, King BJ, & Longhurst CA. (2012). Rapid Implementation of Inpatient Electronic Physician Documentation at an Academic Hospital. Applied Clinical Informatics, 3(2).

Septopreoptic Holoprosencephaly: A Mild Subtype Associated with Midline Craniofacial Anomalies
Hahn, J. S., Barnes, P. D., Clegg, N. J., & Stashinko, E. E. (2010). Septopreoptic Holoprosencephaly: A Mild Subtype Associated with Midline Craniofacial Anomalies. AMERICAN JOURNAL OF NEURORADIOLOGY, 31(9), 1596-1601.

Decrease in Hospital-wide Mortality Rate After Implementation of a Commercially Sold Computerized Physician Order Entry System
Longhurst, C. A., Parast, L., Sandborg, C. I., Widen, E., Sullivan, J., & Sharek, P. J. (2010). Decrease in Hospital-wide Mortality Rate After Implementation of a Commercially Sold Computerized Physician Order Entry System. PEDIATRICS, 126(1), 14-21.

Neuroimaging Advances in Holoprosencephaly: Refining the Spectrum of the Midline Malformation
Hahn, J. S., & Barnes, P. D. (2010). Neuroimaging Advances in Holoprosencephaly: Refining the Spectrum of the Midline Malformation. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 154C(1), 120-132.

Differential diagnosis and evaluation in pediatric multiple sclerosis
Hahn, J. S., Pohl, D., Rensel, M., & Rao, S. (2007). Differential diagnosis and evaluation in pediatric multiple sclerosis. NEUROLOGY, 68, S13-S22.

Acute disseminated encephalomyelitis
Tenembaum, S., Chitnis, T., Ness, J., & Hahn, J. S. (2007). Acute disseminated encephalomyelitis. NEUROLOGY, 68, S23-S36.

Links between abnormal brain structure and cognition in holoprosencephaly
Roesler, C. P., Paterson, S. J., Flax, J., Hahn, J. S., Kovar, C., & Benasich, A. A. (2006). Links between abnormal brain structure and cognition in holoprosencephaly. PEDIATRIC NEUROLOGY, 35(6), 387-394.

Factor analysis of neuroanatomical and clinical characteristics of holoprosencephaly
Hahn, J. S., Barkovich, A. J., Stashinko, E. E., Kinsman, S. L., Delgado, M. R., & Clegg, N. J. (2006). Factor analysis of neuroanatomical and clinical characteristics of holoprosencephaly. BRAIN & DEVELOPMENT, 28(7), 413-419.

Endocrine disorders associated with holoprosencephaly
Hahn, J. S., Hahn, S. M., Kammann, H., Barkovich, A. J., Clegg, N. J., & Levey, E. (2005). Endocrine disorders associated with holoprosencephaly. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 18(10), 935-941.

Evaluation and management of children with holoprosencephaly
Hahn, J. S., & Plawner, L. L. (2004). Evaluation and management of children with holoprosencephaly. PEDIATRIC NEUROLOGY, 31(2), 79-88.

A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly
Stashinko, E. E., Clegg, N. J., Kammann, H. A., Sweet, V. T., Delgado, M. R., & Levey, E. B. (2004). A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 128A(2), 114-119.

Electroencephalography in holoprosencephaly: findings in children without epilepsy
Hahn, J. S., Delgado, M. R., Clegg, N. J., Sparagana, S. P., Gerace, K. L., & Olson, D. M. (2003). Electroencephalography in holoprosencephaly: findings in children without epilepsy. CLINICAL NEUROPHYSIOLOGY, 114(10), 1908-1917.

Hydranencephaly owing to twin-twin transfusion: Serial fetal ultrasonography and magnetic resonance imaging findings
Hahn, J. S., Lewis, A. J., & Barries, P. (2003). Hydranencephaly owing to twin-twin transfusion: Serial fetal ultrasonography and magnetic resonance imaging findings. JOURNAL OF CHILD NEUROLOGY, 18(5), 367-370.

Unilateral schizencephaly and contralateral polymicrogyria associated with umbilical cord mass
Hahn, J. S., & Lewis, A. J. (2003). Unilateral schizencephaly and contralateral polymicrogyria associated with umbilical cord mass. JOURNAL OF CHILD NEUROLOGY, 18(3), 232-234.

MRI shows abnormal white matter maturation in classical holoprosencephaly
Barkovich, A. J., Simon, E. M., Glenn, O. A., Clegg, N. J., Kinsman, S. L., & Hahn, J. S. (2002). MRI shows abnormal white matter maturation in classical holoprosencephaly. NEUROLOGY, 59(12), 1968-1971.

Middle interhemispheric variant of holoprosencephaly - A distinct cliniconeuroradiologic subtype
Lewis, A. J., Simon, E. M., Barkovich, A. J., Clegg, N. J., Delgado, M. R., & Hahn, J. S. (2002). Middle interhemispheric variant of holoprosencephaly - A distinct cliniconeuroradiologic subtype. NEUROLOGY, 59(12), 1860-1865.

Holoprosencephaly: genetic, neuroradiological, and clinical advances.
Hahn, J. S., & Pinter, J. D. (2002). Holoprosencephaly: genetic, neuroradiological, and clinical advances. Seminars in pediatric neurology, 9(4), 309-319.

Neuroanatomy of holoprosencephaly as predictor of function - Beyond the face predicting the brain
Plawner, L. L., Delgado, M. R., Miller, V. S., Levey, E. B., Kinsman, S. L., & Hahn, J. S. (2002). Neuroanatomy of holoprosencephaly as predictor of function - Beyond the face predicting the brain. NEUROLOGY, 59(7), 1058-1066.

The middle interhemispheric variant of holoprosencephaly
Simon, E. M., Hevner, R. F., Pinter, J. D., Clegg, N. J., Delgado, M., & Barkovich, A. J. (2002). The middle interhemispheric variant of holoprosencephaly. AMERICAN JOURNAL OF NEURORADIOLOGY, 23(1), 151-155.

Analysis of the cerebral cortex in holoprosencephaly with attention to the sylvian fissures
Barkovich, A. J., Simon, E. M., Clegg, N. J., Kinsman, S. L., & Hahn, J. S. (2002). Analysis of the cerebral cortex in holoprosencephaly with attention to the sylvian fissures. AMERICAN JOURNAL OF NEURORADIOLOGY, 23(1), 143-150.

Assessment of the deep gray nuclei in holoprosencephaly
Simon, E. M., Hevner, R., Pinter, J. D., Clegg, N. J., Miller, V. S., & Barkovich, A. J. (2000). Assessment of the deep gray nuclei in holoprosencephaly. AMERICAN JOURNAL OF NEURORADIOLOGY, 21(10), 1955-1961.

Holoprosencephaly: recent advances and new insights.
Kinsman, S. L., Plawner, L. L., & Hahn, J. S. (2000). Holoprosencephaly: recent advances and new insights. Current opinion in neurology, 13(2), 127-132.

The impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss
Greene Jessica, Sacks R, Piniewski B, Kil D, & Hahn JS. (2012). The impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss. Journal of Primary Care & Community Health, epublished.

The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss
Jessica Greene, Sacks R, Piniewski B, Kil D, & Hahn JS. (2012). The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss. Journal of Primary Care & Community Health, epublished.

The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss
Jessica Greene, Sacks R, Piniewski B, Kil D, & Hahn JS. (2012). The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss. Journal of Primary Care & Community Health, epublished.

The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss
Jessica Greene, Sacks R, Piniewski B, Kil D, & Hahn JS. (2012). The Impact of an Online Social Network With Wireless Monitoring Devices on Physical Activity and Weight Loss. Journal of Primary Care & Community Health, epublished.

Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals
Solomon, B. D., Lacbawan, F., Mercier, S., Clegg, N. J., Delgado, M. R., & Muenke, M. (2010). Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. JOURNAL OF MEDICAL GENETICS, 47(8), 513-524.

Compound Heterozygosity for Mutations in PAX6 in a Patient With Complex Brain Anomaly, Neonatal Diabetes Mellitus, and Microophthalmia
Solomon, B. D., Pineda-Alvarez, D. E., Balog, J. Z., Hadley, D., Gropman, A. L., & Muenke, M. (2009). Compound Heterozygosity for Mutations in PAX6 in a Patient With Complex Brain Anomaly, Neonatal Diabetes Mellitus, and Microophthalmia. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 149A(11), 2543-2546.

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
Lacbawan, F., Solomon, B. D., ROESSLER, E., El-Jaick, K., Domene, S., & Muenke, M. (2009). Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. JOURNAL OF MEDICAL GENETICS, 46(6), 389-398.

Holoprosencephaly.
Hahn, J. S. (2008). Holoprosencephaly. Handbook of clinical neurology, 87, 13-37.

Functional analysis of mutations in TGIF associated with holoprosencephaly
El-Jaick, K. B., Powers, S. E., Bartholin, L., Myers, K. R., Hahn, J., & Muenke, M. (2007). Functional analysis of mutations in TGIF associated with holoprosencephaly. MOLECULAR GENETICS AND METABOLISM, 90(1), 97-111.

Mild developmental delay in terminal chromosome 6p deletion
Chen, K. M., Cherry, A. M., Hahn, J. S., & Enns, G. M. (2004). Mild developmental delay in terminal chromosome 6p deletion. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 129A(2), 201-205.

Microangiopathy of brain, retina, and inner ear (Susac's syndrome) in an adolescent female presenting as acute disseminated encephalomyelitis
Hahn, J. S., Lannin, W. C., & Sarwal, M. M. (2004). Microangiopathy of brain, retina, and inner ear (Susac's syndrome) in an adolescent female presenting as acute disseminated encephalomyelitis. PEDIATRICS, 114(1), 276-281.

Frontal lobe seizures and uveitis associated with acute human parvovirus B19 infection
Hsu, D., Sandborg, C., & Hahn, J. S. (2004). Frontal lobe seizures and uveitis associated with acute human parvovirus B19 infection. JOURNAL OF CHILD NEUROLOGY, 19(4), 304-306.

Stimulus-induced drop episodes in Coffin-Lowry syndrome
Nelson, G. B., & Hahn, J. S. (2003). Stimulus-induced drop episodes in Coffin-Lowry syndrome. PEDIATRICS, 111(3).

Short duration of benign partial epilepsy in infancy
Nelson, G. B., Olson, D. M., & Hahn, J. S. (2002). Short duration of benign partial epilepsy in infancy. JOURNAL OF CHILD NEUROLOGY, 17(6), 440-445.

Holoprosencephaly: A review
Clegg, N. J., Gerace, K. L., Sparagana, S. P., Hahn, J. S., & Delgado, M. R. (2002). Holoprosencephaly: A review. AMERICAN JOURNAL OF ELECTRONEURODIAGNOSTIC TECHNOLOGY, 42(2), 59-72.

Congenital hypomyelination neuropathy in a newborn infant: Unusual cause of diaphragmatic and vocal cord paralyses
Hahn, J. S., Henry, M., Hudgins, L., & Madan, A. (2001). Congenital hypomyelination neuropathy in a newborn infant: Unusual cause of diaphragmatic and vocal cord paralyses. PEDIATRICS, 108(5).

Sedation of children for electroencephalograms
Olson, D. M., Sheehan, M. G., Thompson, W., Hall, P. T., & Hahn, J. (2001). Sedation of children for electroencephalograms. PEDIATRICS, 108(1), 163-165.

Structured data management - the design and implementation of a web-based video archive prototype
Zou, H., Lu, Q. C., Durack, J. C., Chao, C., Strasberg, H. R., & Hahn, J. S. (2001). Structured data management - the design and implementation of a web-based video archive prototype. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, 786-790.

Moyamoya syndrome in children with Alagille syndrome: Additional evidence of a vasculopathy
Woolfenden, A. R., Albers, G. W., Steinberg, G. K., Hahn, J. S., Johnston, D. Cc., & Farrell, K. (1999). Moyamoya syndrome in children with Alagille syndrome: Additional evidence of a vasculopathy. PEDIATRICS, 103(2), 505-508.

Progressive multifocal leukoencephalopathy in a 15-year-old boy with scleroderma and secondary amyloidosis
Hahn, J. S., Harris, B. T., Gutierrez, K., & Sandborg, C. (1998). Progressive multifocal leukoencephalopathy in a 15-year-old boy with scleroderma and secondary amyloidosis. PEDIATRICS, 102(6), 1475-1479.

Celiac disease presenting as gait disturbance and ataxia in infancy
Hahn, J. S., Sum, J. M., Bass, D., Crowley, R. S., & Horoupian, D. S. (1998). Celiac disease presenting as gait disturbance and ataxia in infancy. JOURNAL OF CHILD NEUROLOGY, 13(7), 351-353.

Wernicke encephalopathy and Beriberi during total parenteral nutrition attributable to multivitamin infusion shortage
Hahn, J. S., Berquist, W., Alcorn, D. M., Chamberlain, L., & Bass, D. (1998). Wernicke encephalopathy and Beriberi during total parenteral nutrition attributable to multivitamin infusion shortage. PEDIATRICS, 101(1).

Bilateral tonic-clonic epileptic seizures in non-benign familial neonatal convulsions
Alfonso, I., Hahn, J. S., Papazian, O., Martinez, Y. L., Reyes, M. A., & Aicardi, J. (1997). Bilateral tonic-clonic epileptic seizures in non-benign familial neonatal convulsions. PEDIATRIC NEUROLOGY, 16(3), 249-251.

Phenytoin-related chorea in children with deep hemispheric vascular malformations
Koukkari, M. W., Vanefsky, M. A., Steinberg, G. K., & Hahn, J. S. (1996). Phenytoin-related chorea in children with deep hemispheric vascular malformations. JOURNAL OF CHILD NEUROLOGY, 11(6), 490-491.

Intravenous gammaglobulin therapy in recurrent acute disseminated encephalomyelitis
Hahn, J. S., Siegler, D. J., & ENZMANN, D. (1996). Intravenous gammaglobulin therapy in recurrent acute disseminated encephalomyelitis. NEUROLOGY, 46(4), 1173-1174.

Predictive value of EEG for outcome and epilepsy following neonatal seizures
ORTIBUS, E. L., Sum, J. M., & Hahn, J. S. (1996). Predictive value of EEG for outcome and epilepsy following neonatal seizures. ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 98(3), 175-185.

BRAIN-STEM MULTIPLE-SCLEROSIS IN AN 11-YEAR-OLD CHILD PRESENTING AS ACUTE DISSEMINATED ENCEPHALOMYELITIS
Mostafapour, S. P., ENZMANN, D., North, W., & Hahn, J. S. (1995). BRAIN-STEM MULTIPLE-SCLEROSIS IN AN 11-YEAR-OLD CHILD PRESENTING AS ACUTE DISSEMINATED ENCEPHALOMYELITIS. JOURNAL OF CHILD NEUROLOGY, 10(6), 476-480.

KERNICTERUS IN A FULL-TERM INFANT
Penn, A. A., Enzmann, D. R., Hahn, J. S., & Stevenson, D. K. (1994). KERNICTERUS IN A FULL-TERM INFANT. PEDIATRICS, 93(6), 1003-1006.

UNUSUAL MRI FINDINGS AFTER STATUS EPILEPTICUS DUE TO CAT-SCRATCH DISEASE
Hahn, J. S., Sum, J. M., & Lee, K. P. (1994). UNUSUAL MRI FINDINGS AFTER STATUS EPILEPTICUS DUE TO CAT-SCRATCH DISEASE. PEDIATRIC NEUROLOGY, 10(3), 255-258.

DISSEMINATED MULTIFOCAL HERPES-ZOSTER LEUKOENCEPHALITIS AND SUBCORTICAL HEMORRHAGE IN AN IMMUNOSUPPRESSED CHILD
Herrold, J. M., & Hahn, J. S. (1994). DISSEMINATED MULTIFOCAL HERPES-ZOSTER LEUKOENCEPHALITIS AND SUBCORTICAL HEMORRHAGE IN AN IMMUNOSUPPRESSED CHILD. JOURNAL OF CHILD NEUROLOGY, 9(1), 56-58.

CONTROVERSIES IN TREATMENT OF NEONATAL SEIZURES
Hahn, J. S. (1993). CONTROVERSIES IN TREATMENT OF NEONATAL SEIZURES. PEDIATRIC NEUROLOGY, 9(4), 330-331.

ELECTROENCEPHALOGRAPHIC AND NEUROIMAGING FINDINGS IN NEONATES UNDERGOING EXTRACORPOREAL MEMBRANE-OXYGENATION
Hahn, J. S., Vaucher, Y., Bejar, R., & Coen, R. W. (1993). ELECTROENCEPHALOGRAPHIC AND NEUROIMAGING FINDINGS IN NEONATES UNDERGOING EXTRACORPOREAL MEMBRANE-OXYGENATION. NEUROPEDIATRICS, 24(1), 19-24.

PROGNOSTIC VALUE OF EEG IN NEONATAL MENINGITIS - RETROSPECTIVE STUDY OF 29 INFANTS
CHEQUER, R. S., Tharp, B. R., Dreimane, D., Hahn, J. S., Clancy, R. R., & Coen, R. W. (1992). PROGNOSTIC VALUE OF EEG IN NEONATAL MENINGITIS - RETROSPECTIVE STUDY OF 29 INFANTS. PEDIATRIC NEUROLOGY, 8(6), 417-422.

DETECTION OF NEONATAL SEIZURES THROUGH COMPUTERIZED EEG ANALYSIS
Liu, A., Hahn, J. S., Heldt, G. P., & Coen, R. W. (1992). DETECTION OF NEONATAL SEIZURES THROUGH COMPUTERIZED EEG ANALYSIS. ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 82(1), 30-37.

NEONATAL SUBEPENDYMAL GIANT-CELL ASTROCYTOMA ASSOCIATED WITH TUBEROUS SCLEROSIS - MRI, CT, AND ULTRASOUND CORRELATION
Hahn, J. S., Bejar, R., & Gladson, C. L. (1991). NEONATAL SUBEPENDYMAL GIANT-CELL ASTROCYTOMA ASSOCIATED WITH TUBEROUS SCLEROSIS - MRI, CT, AND ULTRASOUND CORRELATION. NEUROLOGY, 41(1), 124-128.

Winner of the Brazier Award. The dysmature EEG pattern in infants with bronchopulmonary dysplasia and its prognostic implications.
Hahn, J. S., & Tharp, B. R. (1990). Winner of the Brazier Award. The dysmature EEG pattern in infants with bronchopulmonary dysplasia and its prognostic implications. Electroencephalography and clinical neurophysiology, 76(2), 106-113.

INTERBURST INTERVAL MEASUREMENTS IN THE EEGS OF PREMATURE-INFANTS WITH NORMAL NEUROLOGICAL OUTCOME
Hahn, J. S., Monyer, H., & Tharp, B. R. (1989). INTERBURST INTERVAL MEASUREMENTS IN THE EEGS OF PREMATURE-INFANTS WITH NORMAL NEUROLOGICAL OUTCOME. ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 73(5), 410-418.

NEUROLOGICAL COMPLICATIONS OF HEMOLYTIC-UREMIC SYNDROME
Hahn, J. S., Havens, P. L., Higgins, J. J., OROURKE, P. P., Estroff, J. A., & Strand, R. (1989). NEUROLOGICAL COMPLICATIONS OF HEMOLYTIC-UREMIC SYNDROME. JOURNAL OF CHILD NEUROLOGY, 4(2), 108-113.

LABORATORY AND CLINICAL-VARIABLES TO PREDICT OUTCOME IN HEMOLYTIC-UREMIC SYNDROME
Havens, P. L., OROURKE, P. P., Hahn, J., Higgins, J., & Walker, A. M. (1988). LABORATORY AND CLINICAL-VARIABLES TO PREDICT OUTCOME IN HEMOLYTIC-UREMIC SYNDROME. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 142(9), 961-964.

CENTRAL MAMMALIAN NEURONS NORMALLY RESISTANT TO GLUTAMATE TOXICITY ARE MADE SENSITIVE BY ELEVATED EXTRACELLULAR CA-2+ - TOXICITY IS BLOCKED BY THE N-METHYL-D-ASPARTATE ANTAGONIST MK-801
Hahn, J. S., Aizenman, E., & Lipton, S. A. (1988). CENTRAL MAMMALIAN NEURONS NORMALLY RESISTANT TO GLUTAMATE TOXICITY ARE MADE SENSITIVE BY ELEVATED EXTRACELLULAR CA-2+ - TOXICITY IS BLOCKED BY THE N-METHYL-D-ASPARTATE ANTAGONIST MK-801. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 85(17), 6556-6560.

SERUM SICKNESS TRIGGERED BY ANAPHYLAXIS - A COMPLICATION OF IMMUNOTHERAPY
Umetsu, D. T., Hahn, J. S., PEREZATAYDE, A. R., & Geha, R. S. (1985). SERUM SICKNESS TRIGGERED BY ANAPHYLAXIS - A COMPLICATION OF IMMUNOTHERAPY. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 76(5), 713-718.