Literature DB >> 5000841

[Acromesomelic dwarfism].

P Maroteaux, B Martinelli, E Campailla.   

Abstract

Mesh：

Year:  1971        PMID： 5000841

Source DB:  PubMed          Journal:  Presse Med        ISSN： 0032-7867            Impact factor:   1.228


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  19 in total

1.  Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy.

Authors:  Pai-Ching Huang; Ju-Hsin Chang; Mei-Ling Shen; Kuen-Bao Chen
Journal:  J Anesth       Date:  2012-04-24       Impact factor: 2.078

Review 2.  Perthes' disease: growth and aetiology.

Authors:  R G Burwell
Journal:  Arch Dis Child       Date:  1988-11       Impact factor: 3.791

3.  Peripheral dysplasia. Report of a new genetic syndrome.

Authors:  L Bacha; L Brachimi; K Kozlowski; R Massen; L Morris
Journal:  Pediatr Radiol       Date:  1989

4.  Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience.

Authors:  Pelin Ozlem Simsek-Kiper; Gizem Urel-Demir; Ekim Z Taskiran; Umut Ece Arslan; Banu Nur; Ercan Mihci; Mithat Haliloglu; Yasemin Alanay; Gulen Eda Utine; Koray Boduroglu
Journal:  J Hum Genet       Date:  2020-12-07       Impact factor: 3.172

5.  A possibly new form of familial bone dysplasia resembling dyschondrosteosis.

Authors:  S Fasanelli; G Iannaccone; A Bellussi
Journal:  Pediatr Radiol       Date:  1983

6.  Mesomelic dysplasia--associated with other abnormalities.

Authors:  H Löhr; H R Wiedemann
Journal:  Eur J Pediatr       Date:  1981-11       Impact factor: 3.183

7.  Analogs of C-type natriuretic peptide as a potential new non-surgical treatment strategy in knee osteoarthritis.

Authors:  Ahmet Cevik Tufan
Journal:  J Orthop       Date:  2019-05-25

8.  Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.

Authors:  A G Hunter; M W Thompson
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

9.  Severe short-limb dwarfism resembling Grebe chondrodysplasia.

Authors:  A S Teebi; S A Al-Awadi; J M Opitz; J Spranger
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

10.  Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux.

Authors:  Cynthia F Bartels; Hulya Bükülmez; Pius Padayatti; David K Rhee; Conny van Ravenswaaij-Arts; Richard M Pauli; Stefan Mundlos; David Chitayat; Ling-Yu Shih; Lihadh I Al-Gazali; Sarina Kant; Trevor Cole; Jenny Morton; Valérie Cormier-Daire; Laurence Faivre; Melissa Lees; Jeremy Kirk; Geert R Mortier; Jules Leroy; Bernhard Zabel; Chong Ae Kim; Yanick Crow; Nancy E Braverman; Focco van den Akker; Matthew L Warman
Journal:  Am J Hum Genet       Date:  2004-05-14       Impact factor: 11.025
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