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Items: 1 to 20 of 84

1.

[A further case of congenital generalized dyschondrotheosis, Ollier type].

CARBONELL JUANICO M, VINETA TEIXIDO J.

Rev Esp Pediatr. 1962 Jan-Feb;18:91-9. Spanish. No abstract available.

PMID:
13876464
2.

[Ollier type of dyschondroplasia].

ROCHER HL, AUFFAURE.

Bord Chir. 1953 Jul;3:168-9. Undetermined Language. No abstract available.

PMID:
13106171
3.

[A case of Ollier disease in a 5 and one-half year old child].

Borushko II, Popova LI.

Vopr Okhr Materin Det. 1968 Apr;13(4):84-5. Russian. No abstract available.

PMID:
5703214
4.

[Some considerations on a case of Ollier disease].

QUEIROZ FERREIRA S.

Rev Bras Cir. 1947 Apr;16(4):209-26. Portuguese. No abstract available.

PMID:
20260714
5.

[Congenital generalized dyschondrosteosis, Ollier's type].

CARBONELL JUANICO M, ROCA DE VINALS R, PONS ROVIRA J.

Rev Esp Pediatr. 1957 Jul-Aug;13(76):463-74. Spanish. No abstract available.

PMID:
13485578
6.

[A case of congenital disease of stippled epiphyses].

JARROUSSE J, KERNEIS JP, LERAT MF, HERVOUET F, CAVELLAT L.

Bull Fed Soc Gynecol Obstet Lang Fr. 1958;10(2):203-5. French. No abstract available.

PMID:
13596725
7.

[Case report of congenital dyschondroplasia calcificans].

STOPP H.

Z Arztl Fortbild (Jena). 1957 Mar 1;51(5):196-9. German. No abstract available.

PMID:
13434193
8.

[Unusual case of congenital dyschondroplasia].

PARENZAN L.

Acta Orthop Belg. 1953 Jul;19(5):180-9. Undetermined Language. No abstract available.

PMID:
13091848
9.

[Congenital abnormalities and anomalies. 3. Dyschondrosteosis (Leri-Weil syndrome) with report on an additional case)].

KIRCHMAIR H.

Med Monatsschr. 1962 Mar;16:174-5. German. No abstract available.

PMID:
14456251
10.

Congenital calcific chondrodystrophy; a case report with consideration of etiology.

KREMENS V, ORLOFF TL, RICHMAN EM.

J Albert Einstein Med Cent (Phila). 1955 Aug;3(4):137-44. No abstract available.

PMID:
13263059
11.
12.

A new familial case of spondylo-epi-metaphyseal dysplasia with multiple dislocations Hall type (leptodactylic form).

Rossi M, De Brasi D, Hall CM, Battagliese A, Melis D, Sebastio G, Andria G.

Clin Dysmorphol. 2005 Jan;14(1):13-8.

PMID:
15602087
13.

A case of Schwartz-Jampel syndrome with cleft palate.

Abdel-Aziz M, Azab NA.

Int J Pediatr Otorhinolaryngol. 2009 Nov;73(11):1601-3. doi: 10.1016/j.ijporl.2009.08.012. Epub 2009 Sep 4.

PMID:
19733405
14.

[A CASE OF FAMILIAL DYSCHONDROSTEOSIS ASSOCIATED WITH OTHER MALFORMATIONS AND WITH A CHROMOSOME ABNORMALITY].

BENICHOU C, DELZANT G, PEILLON F, MILYNARSKI JC.

Rev Rhum Mal Osteoartic. 1964 Mar-Apr;31:139-43. French. No abstract available.

PMID:
14162682
15.

ELLIS-VAN CREVELD SYNDROME. REPORT OF ONE CASE ASSOCIATED WITH ABIOTROPHY OF ELASTIC TISSUE IN THE CARDIOVASCULAR SYSTEM.

BEHAR A, RACHMILEWITZ E.

Arch Intern Med. 1964 Apr;113:606-11. No abstract available.

PMID:
14109022
16.

[Generalized chondrodystrophy in children].

MILOSEVIC Dj, MILOSEVIC V.

Srp Arh Celok Lek. 1956 Sep;84(9):1031-7. Undetermined Language. No abstract available.

PMID:
13391277
17.
18.

[SPONDYLOEPIPHYSIAL CHONDROMALACIA--A FORM OF GENERALIZED ENDOCHONDRAL DYSOSTOSES].

FRIED K.

Fortschr Geb Rontgenstr Nuklearmed. 1965 Apr;102:424-34. German. No abstract available.

PMID:
14312510
19.

[DOMINANT HEREDITARY SYNDROME, COMBINING CRANIO-FACIAL DYSOSTOSIS PECULIAR TYPE, GROWTH INSUFFICIENCY OF CHONDRODYSTROPHIC APPEARANCE, AND MASSIVE THICKENING OF OF THE CORTICES OF LONG BONES].

STANESCO V, MAXIMILIAN C, POENARU S, FLOREA I, STANESCO R, IONESCO V, IOANITIU D.

Rev Fr Endocrinol Clin. 1963 May-Jun;4:219-31. French. No abstract available.

PMID:
14049206
20.

Congenital heart disease in an adult with the Ellis-van Creveld syndrome.

TUBBS FE, CREVASSE L, GREEN JR Jr.

Ann Intern Med. 1962 Nov;57:829-34. No abstract available.

PMID:
13994651

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