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MR Imaging Findings in 2 Cases of Late Infantile GM1 Gangliosidosis

American journal of neuroradiology : AJNR, 2009-08, Vol.30 (7), p.1325-1327

2009

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Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome

Neuropediatrics, 2009-08, Vol.40 (3), p.103-111

2009

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Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease

Neuropediatrics, 2009-12, Vol.40 (6), p.291-294

2009

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GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

Clinical genetics, 2007-11, Vol.72 (5), p.427-433

2007

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How to take a sexual health history

Nursing made incredibly easy!, 2016-11, Vol.14 (6), p.6-11

Pessagno, Richard A.

2016

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Age and sex prevalence estimate of Joubert syndrome in Italy

Neurology, 2020-02, Vol.94 (8)

2020

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Don't be embarrassed: taking a sexual health history

Nursing (Jenkintown, Pa.), 2013-09, Vol.43 (9), p.60-64

Pessagno, Richard A

2013

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Tehama-Colusa Serpentinite Mélange: A Remnant of Franciscan Jurassic Oceanic Lithosphere, Northern California

International geology review, 2005-01, Vol.47 (1), p.65-100

2005

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Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disorders

Neuropediatrics, 2005-08, Vol.36 (4), p.265

2005

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Aicardi–Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy

European journal of paediatric neurology, 2008-09, Vol.12 (5), p.408-411

2008

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Using Short-Term Group Psychotherapy as an Evidence-Based Intervention for First-Time Mothers at Risk for Postpartum Depression

Perspectives in psychiatric care, 2013-07, Vol.49 (3), p.202-209

2013

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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1074-1078

2013

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P247 Anti-N-methyl-D-aspartate-receptor (NMDAR) encephalitis in a 4-year-old girl

European journal of paediatric neurology, 2009, Vol.13, p.S98-S98

2009

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Upper Jurassic (Oxfordian) Radiolaria from the Sula Islands (East Indies); their taxonomic, biostratigraphic, chronostratigraphic, and paleobiogeographic significance

Micropaleontology, 2002, Vol.48 (3), p.229-256

2002

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M.P.3.02 Pontocerebellar hypoplasia and severe white matter volume reduction in a lethal case of mitochondrial encephalomyopathy

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.827-827

2007

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Paleogeography of Jurassic fragments in the Caribbean

Tectonics (Washington, D.C.), 1994-06, Vol.13 (3), p.725-732

1994

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FORAMINIFERAL RESPONSE TO HABITAT DISRUPTION: ARROYO COLORADO, TEXAS

Journal of foraminiferal research, 2003-10, Vol.33 (4), p.294-308

Buzas-Stephens, P.

2003

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IAP019 Aicardi-Goutières syndrome presenting as a late onset sub-acute leukoencephalopathy

European journal of paediatric neurology, 2007, Vol.11, p.60-60

2007

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IAP042 Opsoclonus-Myoclonus-Ataxia: neuropsychological and neuroradiological sequelae

European journal of paediatric neurology, 2007, Vol.11, p.97-97

2007

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Jurassic radiolarite pulses from the Dorsale Calcaire (internal Rif, Morocco): A clue for correlating and interpreting the Tethyan radiolarites

Stratigraphy, 2009, Vol.6 (4), p.277-312

2009

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Jurassic Radiolaria from the Josephine Ophiolite and Overlying Strata, Smith River Subterrane (Klamath Mountains), Northwestern California and Southwestern Oregon

Micropaleontology, 1993, Vol.39 (2), p.93

1993

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Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6

Biochemical and biophysical research communications, 2009-02, Vol.379 (4), p.892-897

2009

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High frequency of mosaic CREBBP deletions in Rubinstein–Taybi syndrome patients and mapping of somatic and germ-line breakpoints

Genomics (San Diego, Calif.), 2007-11, Vol.90 (5), p.567-573

2007

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Long-lasting myopathy as a major clinical feature of sarcoidosis in a child: case report with a 7-year follow-up

Sarcoidosis, vasculitis, and diffuse lung diseases, 2001-06, Vol.18 (2), p.196

2001

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MR Imaging Findings in 2 Cases of Late Infantile GM1 Gangliosidosis

Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome

Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

How to take a sexual health history

Age and sex prevalence estimate of Joubert syndrome in Italy

Don't be embarrassed: taking a sexual health history

Tehama-Colusa Serpentinite Mélange: A Remnant of Franciscan Jurassic Oceanic Lithosphere, Northern California

Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disorders

Aicardi–Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy

Using Short-Term Group Psychotherapy as an Evidence-Based Intervention for First-Time Mothers at Risk for Postpartum Depression

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

P247 Anti-N-methyl-D-aspartate-receptor (NMDAR) encephalitis in a 4-year-old girl

Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies

Upper Jurassic (Oxfordian) Radiolaria from the Sula Islands (East Indies); their taxonomic, biostratigraphic, chronostratigraphic, and paleobiogeographic significance

M.P.3.02 Pontocerebellar hypoplasia and severe white matter volume reduction in a lethal case of mitochondrial encephalomyopathy

Paleogeography of Jurassic fragments in the Caribbean

FORAMINIFERAL RESPONSE TO HABITAT DISRUPTION: ARROYO COLORADO, TEXAS

IAP019 Aicardi-Goutières syndrome presenting as a late onset sub-acute leukoencephalopathy

IAP042 Opsoclonus-Myoclonus-Ataxia: neuropsychological and neuroradiological sequelae

Jurassic radiolarite pulses from the Dorsale Calcaire (internal Rif, Morocco): A clue for correlating and interpreting the Tethyan radiolarites

Jurassic Radiolaria from the Josephine Ophiolite and Overlying Strata, Smith River Subterrane (Klamath Mountains), Northwestern California and Southwestern Oregon

Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6

High frequency of mosaic CREBBP deletions in Rubinstein–Taybi syndrome patients and mapping of somatic and germ-line breakpoints

Long-lasting myopathy as a major clinical feature of sarcoidosis in a child: case report with a 7-year follow-up

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