These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 2328408)

  • 1. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.
    Ben Hamida M; Hentati F; Ben Hamida C
    Brain; 1990 Apr; 113 ( Pt 2)():347-63. PubMed ID: 2328408
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Juvenile amyotrophic lateral sclerosis. Study of 43 cases].
    Ben Hamida M; Hentati F; Ben Hamida C
    Bull Acad Natl Med; 1992 Feb; 176(2):213-9; discussion 219-22. PubMed ID: 1633561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Two cases of familial amyotrophic lateral sclerosis with a SOD1L126S mutation showing high age at onset and slow progression].
    Iwashima T; Tateishi T; Yamasaki R; Motomura K; Ohyagi Y; Kira J
    Rinsho Shinkeigaku; 2010 Mar; 50(3):163-7. PubMed ID: 20235485
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset spastic paraplegia type 10 (SPG10) family presenting with bulbar symptoms and fasciculations mimicking amyotrophic lateral sclerosis.
    Kaji S; Kawarai T; Miyamoto R; Nodera H; Pedace L; Orlacchio A; Izumi Y; Takahashi R; Kaji R
    J Neurol Sci; 2016 May; 364():45-9. PubMed ID: 27084214
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Two cases of familial spastic paraparesis with amyotrophy of the hands].
    Yamada T; Tashiro K; Moriwaka F; Fujiki N; Ito K; Honma S; Matsuura T; Doi S
    No To Shinkei; 1989 Jun; 41(6):583-8. PubMed ID: 2679823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant juvenile amyotrophic lateral sclerosis.
    Rabin BA; Griffin JW; Crain BJ; Scavina M; Chance PF; Cornblath DR
    Brain; 1999 Aug; 122 ( Pt 8)():1539-50. PubMed ID: 10430837
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The diagnosis of amyotrophic lateral sclerosis supported by motor evoked potential and brain MRI studies].
    Matsunaga K; Iwamoto M; Tsuji S; Hashimoto T; Murai Y
    Rinsho Shinkeigaku; 1997 Mar; 37(3):233-8. PubMed ID: 9217423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)].
    Feki I; Miladi MI; Elleuch N; Boukhris A; Stévanin G; Brice A; Mhiri C
    Rev Neurol (Paris); 2007 Apr; 163(4):476-9. PubMed ID: 17452950
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?
    De Jonghe P; Auer-Grumbach M; Irobi J; Wagner K; Plecko B; Kennerson M; Zhu D; De Vriendt E; Van Gerwen V; Nicholson G; Hartung HP; Timmerman V
    Brain; 2002 Jun; 125(Pt 6):1320-5. PubMed ID: 12023320
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A amyotrophic lateral sclerosis (ALS) 4 family misdiagnosed as hereditary spastic paraplegia-a case report].
    Taniguchi T; Hokezu Y; Okada T; Ishibashi M; Hashiguchi A; Matsuura E; Takashima H
    Rinsho Shinkeigaku; 2017 Nov; 57(11):685-690. PubMed ID: 29070749
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Peroneal muscle atrophy with talipes cavus. Pyramidal symptoms and sensory disorders in one family. On the problem of the nosological classification of hereditary spinal diseases and polyneuropathies].
    Schnider A; Hess CW; Meier C
    Schweiz Med Wochenschr; 1990 Nov; 120(47):1755-62. PubMed ID: 2255880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Stark-Kaeser type of chronic scapulo-peroneal amyotrophy. Apropos of 10 cases].
    Serratrice G; Gastaut JL; Pellissier JF; Pouget J
    Rev Neurol (Paris); 1976 Dec; 132(12):823-32. PubMed ID: 1013569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial amyotrophic lateral sclerosis. Report of a family with predominant upper limb pareses and late onset.
    Hestnes A; Mellgren SI
    Acta Neurol Scand; 1980 Mar; 61(3):192-9. PubMed ID: 7395463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial spastic paraplegia with amyotrophy. Clinical, electromyographic, histochemical study and microdissection].
    Werneck LC; Sanches MC
    Arq Neuropsiquiatr; 1979 Jun; 37(2):138-50. PubMed ID: 91360
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial amyotrophic lateral sclerosis with rapid progression].
    Oyama G; Izawa N; Fujishima K; Kobayashi H; Mizuno Y; Okuma Y
    No To Shinkei; 2005 Nov; 57(11):1003-6. PubMed ID: 16363640
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A patient with motor neuron syndrome clinically similar to amyotrophic lateral sclerosis, presenting spontaneous recovery].
    Miyoshi K; Ohyagi Y; Amano T; Inoue I; Miyoshi S; Tsuji S; Yamada T; Kira J
    Rinsho Shinkeigaku; 2000 Nov; 40(11):1090-5. PubMed ID: 11332188
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial progressive bulbar and spinal muscular atrophy. Juvenile onset and late morbidity with ragged-red fibers.
    Dobkin BH; Verity MA
    Neurology; 1976 Aug; 26(8):754-63. PubMed ID: 945870
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Benign monomelic amyotrophy of lower limb: report of three cases.
    Uncini A; Servidei S; Delli Pizzi C; Cutarella R; Di Muzio A; Gambi D; Tonali P
    Acta Neurol Scand; 1992 Jun; 85(6):397-400. PubMed ID: 1642110
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional compensation in partially denervated muscles.
    McComas AJ; Sica RE; Campbell MJ; Upton AR
    J Neurol Neurosurg Psychiatry; 1971 Aug; 34(4):453-60. PubMed ID: 4938133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Systemic diseases of the motor neurons. Amyotrophic lateral sclerosis, spinal progressive muscular atrophy, progressive bulbar paralysis, spastic spinal paralysis, peripheral nerve muscular atrophy].
    HIRAYAMA K
    Naika; 1962 Dec; 10():1067-9. PubMed ID: 13954748
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.