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Literature DB >> 14172969

CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

Abstract

Entities: Disease

Keywords: ABNORMALITIES; ANATOMY; CHILD; GENETICS, HUMAN; MEDULLA OBLONGATA; MENTAL RETARDATION; PATHOLOGY; VOCAL CORD PARALYSIS

Mesh：

Year: 1964 PMID： 14172969 DOI： 10.1056/NEJM196409172711203

Source DB: PubMed Journal: N Engl J Med ISSN： 0028-4793 Impact factor: 91.245

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Cited

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12 in total

1. OBSERVATIONS ON THE PATHOLOGY OF THE MOEBIUS SYNDROME.

Authors: S E PITNER; J E EDWARDS; W F MCCORMICK
Journal: J Neurol Neurosurg Psychiatry Date: 1965-08 Impact factor: 10.154

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. [Pathophysiology of stenoses of larynx and trachea].

Authors: B Minnigerode
Journal: Arch Klin Exp Ohren Nasen Kehlkopfheilkd Date: 1971

4. Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family.

Authors: G Morelli; C Mesolella; M L Cavaliere; M Stabile; V Ventruto
Journal: J Med Genet Date: 1980-08 Impact factor: 6.318

5. 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

6. 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

CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

1. OBSERVATIONS ON THE PATHOLOGY OF THE MOEBIUS SYNDROME.

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

3. [Pathophysiology of stenoses of larynx and trachea].

4. Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family.

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

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

7. Neonatal Stridor in Familial Congenital Laryngeal Paralysis (Plott Syndrome):  A Case Study in an Omani Family.

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

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

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