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Items: 1 to 20 of 134

1.

[FAMILIAL SYNDROME COMBINING ATAXIA, DEAFNESS AND OLIGOPHRENIA. MYOCARDIAL SCLEROSIS WITH FATAL DEVELOPMENT IN ONE OF THE CHILDREN].

JEUNE M, TOMMASI M, FREYCON F, NIVELON JL.

Pediatrie. 1963;18:984-7. French. No abstract available.

PMID:
14105581
2.

[HEREDITARY CEREBELLO-LENTAL DEGENERATION WITH OLIGOPHRENIA (SO-CALLED MARINESCO-SJOEGREN SYNDROME)].

MATTYUS A, BOHAR A, KISZELY K.

Psychiatr Neurol (Basel). 1965;149:115-25. German. No abstract available.

PMID:
14311323
3.

[OLIGOPHRENIA, ATAXIA, BILATERAL CATARACT (MARINESCO-SJOEGREN SYNDROME) ASSOCIATED WITH CONGENITAL TOXOPLASMOSIS].

ZLATOVEROV AI, IARTSEVA LV, KRSILNIKOVA NA.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1963;63:1478-81. Russian. No abstract available.

PMID:
14183977
4.
6.

REFSUM'S SYNDROME: REPORT OF A CASE INCLUDING ELECTRON MICROSCOPIC STUDIES OF THE LIVER.

KOLODNY EH, HASS WK, LANE B, DRUCKER WD.

Arch Neurol. 1965 Jun;12:583-96. No abstract available.

PMID:
14295958
7.

A new form of familial ataxia, deafness, and mental retardation.

Reardon W, Wilson J, Cavanagh N, Baraitser M.

J Med Genet. 1993 Aug;30(8):694-5.

8.

MENTAL RETARDATION: METHODS OF DIAGNOSIS AND SOME RECENTLY DESCRIBED SYNDROMES.

RICHARDS BW.

Can Med Assoc J. 1963 Nov 16;89:1024-9. Review.

9.

ABNORMALITIES OF SERUM GAMMA-1-A GLOBULIN AND ATAXIA TELANGIECTASIA.

YOUNG RR, AUSTEN KF, MOSER HW.

Medicine (Baltimore). 1964 May;43:423-33. No abstract available.

PMID:
14168753
10.

COCKAYNE'S SYNDROME. A REPORT OF FIVE NEW CASES WITH BIOCHEMICAL, CHROMOSOMAL, DERMATOLOGIC, GENETIC AND NEUROPATHOLOGIC OBSERVATIONS.

PADDISON RM, MOOSSY J, DERBES VJ, KLOEPFER W.

Dermatol Trop Ecol Geogr. 1963 Oct-Dec;15:195-203. No abstract available.

PMID:
14156156
11.

[ATAXIA-TELANGIECTASIA. CONSIDERATIONS ON 2 FAMILIAL CASES].

PEREZSOLER A, ESPADALER JM.

Rev Esp Otoneurooftalmol Neurocir. 1964 May-Jun;23:166-78. Spanish. No abstract available.

PMID:
14205811
12.

THE MARINESCO-SJOEGREN SYNDROME.

NORWOOD WF Jr.

J Pediatr. 1964 Sep;65:431-7. No abstract available.

PMID:
14210863
13.

[Richards-Rundle syndrome].

Fehlow P, Walther F.

Klin Padiatr. 1991 May-Jun;203(3):184-6. German.

PMID:
1857055
14.

THE SYNDROME OF PROGRESSIVE CEREBRAL POLIODYSTROPHY.

GREENHOUSE AH, NEUBUERGER KT.

Arch Neurol. 1964 Jan;10:47-57. No abstract available.

PMID:
14089376
15.

[LEPRECHAUNISM. (APROPOS OF A LITTLE KNOWN FORM OF FAMILIAL OLIGOPHRENIA)].

BAMATTER F.

Rev Med Suisse Romande. 1964 Jun;84:494-502. French. No abstract available.

PMID:
14187829
16.

SENSORY NEURAL DEAFNESS.

PERLMAN HB.

Arch Otolaryngol. 1964 May;79:534-9. No abstract available.

PMID:
14120679
17.

[MOSAIC TRISOMY D1/ NORMAL IN A 6-YEAR-OLD GIRL WITH AN INCOMPLETE SYNDROME OF TRISOMY D1].

FORTEZA G, BAGUENA R, AMAT E, BARCIA D, JUAN A.

Med Esp. 1964 Feb;51:83-93. Spanish. No abstract available.

PMID:
14138513
18.

CONGENITAL LIPODYSTROPHIC DIABETES WITH ACANTHOSIS NIGRICANS: THE SEIP-LAWRENCE SYNDROME.

REED WB, DEXTER R, CORLEY C, FISH C.

Arch Dermatol. 1965 Apr;91:326-34. No abstract available.

PMID:
14275494
19.

[THE ELECTROENCEPHALOGRAM IN FAMILIAL HEREDITARY RETINITIS PIGMENTOSA].

PARIANTE F, TURCHIARO GG.

Osp Psichiatr. 1963 Jan-Sep;31:169-86. Italian. No abstract available.

PMID:
14166336
20.

[THE NEPHROPATHY-DEAFNESS FAMILIAL SYNDROME].

GUERRIER Y, DEJEAN Y.

Rev Laryngol Otol Rhinol (Bord). 1964 Oct;85:SUPPL:925-35. French. No abstract available.

PMID:
14243565

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