Literature DB >> 4751313

Familial laryngeal abductor paralysis and psychomotor retardation.

G V Watters, N Fitch.   

Abstract

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Year:  1973        PMID： 4751313     DOI： 10.1111/j.1399-0004.1973.tb01172.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  8 in total

1.  Anatomical progression of the Chiari II malformation.

Authors:  J R Ruge; J Masciopinto; B B Storrs; D G McLone
Journal:  Childs Nerv Syst       Date:  1992-03       Impact factor: 1.475

2.  Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?

Authors:  E Boltshauser; W Lang; T Spillmann; E Hof
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

3.  Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected.

Authors:  A Schinzel; E Hof; P Dangel; W Robinson
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

4.  Distal spinal and bulbar muscular atrophy caused by dynactin mutation.

Authors:  Imke Puls; Shin J Oh; Charlotte J Sumner; Karen E Wallace; Mary Kay Floeter; Eric A Mann; William R Kennedy; Gwen Wendelschafer-Crabb; Alexander Vortmeyer; Richard Powers; Kimberly Finnegan; Erika L F Holzbaur; Kenneth H Fischbeck; Christy L Ludlow
Journal:  Ann Neurol       Date:  2005-05       Impact factor: 10.422

5.  Paradoxical vocal cord movement in newborn and congenital idiopathic vocal cord paralysis: two of a kind?

Authors:  Turid Omland; Kjell Brøndbo
Journal:  Eur Arch Otorhinolaryngol       Date:  2008-04-18       Impact factor: 2.503

6.  Hereditary distal spinal muscular atrophy with vocal cord paralysis.

Authors:  I D Young; P S Harper
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-05       Impact factor: 10.154

7.  Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins.

Authors:  W O Renier; F J Gabreëls; T W Hustinx; H H Jaspar; J A Geelen; U J Van Haelst; E J Lommen; B G Ter Haar
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

8.  Xq27.1 palindrome mediated interchromosomal insertion likely causes familial congenital bilateral laryngeal abductor paralysis (Plott syndrome).

Authors:  Felix Boschann; Daniel Acero Moreno; Martin A Mensah; Henrike L Sczakiel; Karolina Skipalova; Manuel Holtgrewe; Stefan Mundlos; Björn Fischer-Zirnsak
Journal:  J Hum Genet       Date:  2022-01-31       Impact factor: 3.755
  8 in total

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