List of bibliographic references indexed by 1432-1076
Number of relevant bibliographic references: 25.
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| Ident. | Authors (with country if any) | Title |
|---|
| 000567 (2017) |
Aisling M. O'Riordan [Irlande (pays)] ; Niamh Mcgrath [Irlande (pays)] ; Farhana Sharif [Irlande (pays)] ; Nuala P. Murphy [Irlande (pays)] ; Orla Franklin [Irlande (pays)] ; Sally Ann Lynch [Irlande (pays)] ; Michael J. O'Grady [Irlande (pays)] | Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance. |
| 002047 (2015) |
Michaela Kuhlen [Allemagne] ; Arndt Borkhardt [Allemagne] | Cancer susceptibility syndromes in children in the area of broad clinical use of massive parallel sequencing |
| 004257 (2012) |
Gwendolyn De Bruyn [Belgique] ; Alexandra Casaer ; Katrien Devolder ; Geert Van Acker ; Hilde Logghe ; Koen Devriendt ; Luc Cornette | Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression. |
| 004290 (2012) |
Hiroyuki Ishida [Japon] ; Kosuke Imai ; Kenichi Honma ; Shin-Ichi Tamura ; Toshihiko Imamura ; Masafumi Ito ; Shigeaki Nonoyama | GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. |
| 004F29 (2011) |
Rogier Kersseboom [Pays-Bas] ; Alice Brooks [Pays-Bas] ; Corry Weemaes [Pays-Bas] | Educational paper |
| 005A58 (2010) |
Catherine M L. Roberts [Royaume-Uni] ; Janet E. Angus ; Ian H. Leach ; Elizabeth M. Mcdermott ; David A. Walker ; Jane C. Ravenscroft | A novel NEMO gene mutation causing osteopetrosis, lymphoedema, hypohidrotic ectodermal dysplasia and immunodeficiency (OL-HED-ID). |
| 00C486 (1995) |
G. Haeusler [Autriche] ; H. Frisch [Autriche] ; K. Schmitt [Autriche] ; P. Blümel [Autriche] ; E. Plöchl [Autriche] ; M. Zachmann [Suisse] ; T. Waldhör [Autriche] | Treatment of patients with Ullrich-Turner syndrome with conventional doses of growth hormone and the combination with testosterone or oxandrolone: Effect on growth, IGF-I and IGFBP-3 concentrations |
| 00C615 (1995) |
I. E. Alexander [Australie] ; G. P. Tauro [Australie] ; A. Bankier [Australie] | Fetal brain disruption sequence in sisters |
| 00CA66 (1994) |
Rune W. Naeraa [Danemark] ; Johannes Nielsen [Danemark] ; Knud W. Kastrup [Danemark] | Growth hormone and 17β-oestradiol treatment of Turner girls — 2-year results |
| 00CA94 (1994) |
C. W. M. Verlaat [Pays-Bas] ; H. M. Peters [Pays-Bas] ; B. A. Semmekrot [Pays-Bas] ; J. M. Wiersma-Van Tilburg [Pays-Bas] | Congenital pulmonary lymphangiectasis presenting as a unilateral hyperlucent lung |
| 00CB17 (1994) |
J. C. Craig [Australie] ; W. G. Grigor [Australie] ; J. F. Knight [Australie] | Acute obstructive uropathy —a rare complication of circumcision |
| 00CE86 (1993) |
W. Wiebicke [Allemagne] ; A. Artlich [Allemagne] ; I. Gerling [Allemagne] | Myocardial fibrosis — a rare complication in patients with cystic fibrosis |
| 00D804 (1991) |
D. M. Danks [Australie] | Copper and liver disease |
| 00DB71 (1990) |
M. Pery [Israël] ; U. Alon [Israël] ; J. H. Lachter [Israël] ; J. K. Kaftori [Israël] ; D. Gaitini [Israël] ; A. Rosenberger [Israël] | The value of ultrasound in Schoenlein-Henoch purpura |
| 00EB38 (1986) |
D. M. Smeltzer [États-Unis] ; G. B. Stickler [États-Unis] ; R. E. Fleming [États-Unis] | Primary lymphatic dysplasia in children: chylothorax, chylous ascites, and generalized lymphatic dysplasia |
| 00EB96 (1986) |
J. Mücke ; W. Hoepffner ; G. Scheerschmidt ; H. Gornig ; K. Beyreiss | Early onset lymphoedema, recessive form — a new form of genetic lymphoedema syndrome |
| 00EE78 (1985) |
J. R. Casley-Smith [Australie] | The importance of the lymphatic system |
| 00EF87 (1985) |
R. A. Kroczek [Allemagne] | Congenital chyloperitoneum: direct comparison of medium-chain triglyceride treatment with total parenteral nutrition |
| 00F002 (1985) |
Shigeru Tomita [Japon] ; Toru Kurokawa [Japon] ; Kohji Ueda [Japon] ; Shun Higuchi [Japon] | Aplastic anaemia induced by intravenous phenytoin and lidocaine administration |
| 00F732 (1982) |
E. Fisher [États-Unis] ; E. B. Weiss [États-Unis] ; K. Michals [États-Unis] ; I. W. Dubrow [États-Unis] ; A. R. Hastrieter [États-Unis] ; R. Matalon [États-Unis] | Spontaneous chylothorax in Noonan's syndrome |
| 00F805 (1982) |
J. Kunze ; H. Riehm | A new genetic disorder: Autosomal-dominant multiple benign ring-shaped skin creases |
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