Evaluation and management of children with holoprosencephaly

scientific article published in August 2004

Evaluation and management of children with holoprosencephaly is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1016/J.PEDIATRNEUROL.2004.03.006
P698PubMed publication ID15301825
P5875ResearchGate publication ID8408996

P2093author name stringJin S Hahn
Lauren L Plawner
P433issue2
P921main subjectholoprosencephalyQ1459821
P304page(s)79-88
P577publication date2004-08-01
P1433published inPediatric NeurologyQ15752159
P1476titleEvaluation and management of children with holoprosencephaly
P478volume31

Reverse relations

cites work (P2860)
Q53214629A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum.
Q33718429A preterm infant with semilobar holoprosencephaly and hydrocephalus: a case report
Q56261843Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review
Q41936304Clinical Features and Outcomes of Holoprosencephaly in Korea
Q33624701Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients
Q38071553Diffusion tensor imaging and fiber tractography in brain malformations
Q31097430Holoprosencephaly
Q82029948Holoprosencephaly
Q92583817Holoprosencephaly-Associated Hyperkinesia
Q34041428Holoprosencephaly: a guide to diagnosis and clinical management
Q35973166Links between abnormal brain structure and cognition in holoprosencephaly
Q33842657Magnetic resonance imaging of intracranial malformations in dogs and cats
Q42509637Multisystem Involvement in a Patient with a PTCH1 Mutation: Clinical and Imaging Findings
Q36068557New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases
Q48494005Rare Disease: Lobar Holoprosencephaly With a Median Cleft Lip-Case Report
Q41177792Semilobarholoprosencephaly - A Dreading Congenital Anomaly
Q34329523The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes

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