Sage Journals: Discover world-class research

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Research article

First published 1996-08

The Human Mandibular Canal Arises from Three Separate Canals Innervating Different Tooth Groups

M.E. Chávez-Lomelí, J. Mansilla Lory, J.A. Pompa [...]

Journal of Dental Research

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Research article

First published 2017-9

Postmortem Whole Exome Sequencing Identifies Novel EIF2B3 Mutation With Prenatal Phenotype in 2 Siblings

Hannah Song, Sina Haeri, Hannes Vogel [...]

Journal of Child Neurology

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Research article

First published 1997-7

Optic Nerve Hypoplasia in Fetal Alcohol Syndrome: An Update

M.D. Pinazo-Duran, J. Renau-Piqueras, C. Guerri [...]

European Journal of Ophthalmology

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Research article

First published 2005-11

Nonsyndromic Isolated Unilateral Cochlear Nerve Aplasia without Narrow Internal Auditory Meatus: A Previously Overlooked Cause of Unilateral Profound Deafness in Childhood

Ken Ito, Asayo Endo, Hiroko Monobe [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 1990-1

Insulin-like growth factor II gene expression: relationship to the development and regeneration of neuromuscular synapses

Douglas N. Ishii

Restorative Neurology and Neuroscience

Free access

Research article

First published 2016-11-29

Type 0 Spinal Muscular Atrophy: Further Delineation of Prenatal and Postnatal Features in 16 Patients

Sarah Grotto, Jean-Marie Cuisset, Stéphane Marret [...]

Journal of Neuromuscular Diseases

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Research article

First published 2017-3

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature

Sylvie Picker-Minh, Sebastian Hartenstein, Hans Proquitté [...]

Journal of Child Neurology

Open access

Case report

First published 2024-3

Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Disease

Sini Keskinen, Teija Paakkola, Mirjami Mattila [...]

Pediatric and Developmental Pathology

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Research article

First published 1994-10

Atelencephalic Aprosencephaly

Cheryl P. Harris, Jeannette J. Townsend, Margaret G. Norman [...]

Journal of Child Neurology

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Case report

First published 2018-5

Postmortem Diagnostic Exome Sequencing Identifies a De Novo TUBB3 Alteration in a Newborn With Prenatally Diagnosed Hydrocephalus and Suspected Walker–Warburg Syndrome

Zöe Powis, Adam C Chamberlin, Christina L Alamillo [...]

Pediatric and Developmental Pathology

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