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Items: 1 to 20 of 77

1.

Familial brachyolmia.

Darcan S, Yalman O, Coker M, Demir N, Ozkinay F.

J Pediatr Endocrinol Metab. 2000 Jul-Aug;13(7):955-8.

PMID:
10968486
2.
3.

Growth hormone secretory pattern and response to treatment in children with short stature followed to adult height.

Radetti G, Buzi F, Cassar W, Paganini C, Stacul E, Maghnie M.

Clin Endocrinol (Oxf). 2003 Jul;59(1):27-33.

PMID:
12807500
4.

Brachyolmia and spinal stenosis.

Mukamel M, Karmazyn B, de Vries L, Horev G, Shohat M.

Am J Med Genet A. 2003 Jul 15;120A(2):272-5.

PMID:
12833413
5.

Spondyloenchondrodysplasia: clinical variability in three cases.

Tüysüz B, Arapoglu M, Ungür S.

Am J Med Genet A. 2004 Jul 15;128A(2):185-9.

PMID:
15214014
6.

[Brachyolmia at autosomal recessive transmission].

Soua H, Sassi N, Karboul L, Ayadi A, Boussoffara R, Belkhir Y, Lengliz N, Hamza H, Sfar MT, Maroteaux P.

Arch Pediatr. 1994 May;1(5):505-7. French.

PMID:
7951838
8.
9.

Stature and severity in multiple epiphyseal dysplasia.

Haga N, Nakamura K, Takikawa K, Manabe N, Ikegawa S, Kimizuka M.

J Pediatr Orthop. 1998 May-Jun;18(3):394-7.

PMID:
9600570
10.

Two sibs with brachyolmia type Hobaek: five year follow-up through puberty.

Hoo JJ, Oliphant M.

Am J Med Genet A. 2003 Jan 1;116A(1):80-4.

PMID:
12476457
11.

[Schimke immuno-osseous dysplasia].

Stajić N, Rajić V, Zdravković D, Marjanović B, Zamurović D, Gujanica Z, Vlahović G, Bogdanović R.

Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:63-7. Serbian.

PMID:
15637995
12.

Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.

Opitz JM, Spranger JW, Stöss HR, Pesch HJ, Azadeh B.

Am J Med Genet. 1987 Mar;26(3):583-90.

PMID:
3565474
13.

Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry.

Wajnrajch MP, Gertner JM, Huma Z, Popovic J, Lin K, Verlander PC, Batish SD, Giampietro PF, Davis JG, New MI, Auerbach AD.

Pediatrics. 2001 Apr;107(4):744-54.

PMID:
11335753
14.

High bone mineral density in pycnodysostotic patients with a novel mutation in the propeptide of cathepsin K.

Schilling AF, Mülhausen C, Lehmann W, Santer R, Schinke T, Rueger JM, Amling M.

Osteoporos Int. 2007 May;18(5):659-69. Epub 2007 Jan 6.

PMID:
17206399
15.

A case of brachyolmia.

Karabiyik N, Oğuz F, Sidal M, Hekim N, Kayserili H.

Turk J Pediatr. 1997 Jul-Sep;39(3):415-20.

PMID:
9339123
17.

Autosomal dominant brachyolmia in a large Swedish family: phenotypic spectrum and natural course.

Grigelioniene G, Geiberger S, Horemuzova E, Moström E, Jäntti N, Neumeyer L, Åström E, Nordenskjöld M, Nordgren A, Mäkitie O.

Am J Med Genet A. 2014 Jul;164A(7):1635-41. doi: 10.1002/ajmg.a.36502. Epub 2014 Mar 26. Review.

PMID:
24677493
18.

Melnick-Needles syndrome and GH-deficiency: a possible new association feature.

Femiano P, Castaldo V, Iossa C, Pascarella F.

Minerva Pediatr. 2005 Dec;57(6):419-22.

PMID:
16402013
19.

Target height estimation in children with idiopathic short stature who are referred to the growth clinic.

Poyrazoglu S, Darendeliler F, Bas F, Bundak R, Saka N, Darcan S, Wit JM, Gunoz H.

Horm Res. 2009;72(3):178-83. doi: 10.1159/000232494. Epub 2009 Sep 1.

PMID:
19729950
20.

An effective case of growth hormone treatment on cartilage-hair hypoplasia.

Harada D, Yamanaka Y, Ueda K, Shimizu J, Inoue M, Seino Y, Tanaka H.

Bone. 2005 Feb;36(2):317-22.

PMID:
15780958

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