(Q28292924)

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Neurosurgical aspects of childhood hypophosphatasia

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scholarly article

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Neurosurgical aspects of childhood hypophosphatasia (English)

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hypophosphatasia

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childhood hypophosphatasia

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based on heuristic

inferred from title

author name string

H Collmann

1

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E Mornet

2

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S Gattenlöhner

3

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C Beck

4

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H Girschick

5

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language of work or name

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publication date

February 2009

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Child's Nervous System

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25

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2

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217-23

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https://scigraph.springernature.com/pub.10.1007/s00381-008-0708-3

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Hypophosphatasia

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https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype-phenotype correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture

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https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radiographic manifestations of congenital anomalies of the skull

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https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glu274Lys/Gly309Arg mutation of the tissue-nonspecific alkaline phosphatase gene in neonatal hypophosphatasia associated with convulsions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hydrocephalus in craniosynostosis: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

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inferred from PubMed ID database lookup

Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term follow-up of bone mineral density in childhood hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

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Hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypophosphatasia. Review of 24 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilambdoid and posterior sagittal synostosis: the Mercedes Benz syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis and functional correlation with phenotype in German patients with childhood-type hypophosphatasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18769927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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