-
2
-
-
0026350171
-
Pituitary evaluation and growth hormone treatment in Prader-Willi syndrome
-
Angulo M., Castro-Magana M. & Uly J. (1991) Pituitary evaluation and growth hormone treatment in Prader-Willi syndrome. Journal of Pediatric Endocrinology 3, 167-73.
-
(1991)
Journal of Pediatric Endocrinology
, vol.3
, pp. 167-173
-
-
Angulo, M.1
Castro-Magana, M.2
Uly, J.3
-
3
-
-
0037065539
-
Psychotic illness in people with Prader-Willi syndrome due to chromosome 15 maternal uniparental disomy
-
Boer H., Holland A., Whittington J., Butler J., Webb T. & Clarke D. (2002) Psychotic illness in people with Prader-Willi syndrome due to chromosome 15 maternal uniparental disomy. The Lancet 359, 135-6.
-
(2002)
The Lancet
, vol.359
, pp. 135-136
-
-
Boer, H.1
Holland, A.2
Whittington, J.3
Butler, J.4
Webb, T.5
Clarke, D.6
-
4
-
-
0031984133
-
Incidence of selective serotonin reuptake inhibitor (SSRI) induced hyponatremia due to the syndrome of inappropriate antidiuretic hormone (SIADH) secretion in the elderly
-
Bouman W. P., Pinner G. & Johnson H. (1998) Incidence of selective serotonin reuptake inhibitor (SSRI) induced hyponatremia due to the syndrome of inappropriate antidiuretic hormone (SIADH) secretion in the elderly. International Journal of Geriatric Psychiatry 13, 12-15.
-
(1998)
International Journal of Geriatric Psychiatry
, vol.13
, pp. 12-15
-
-
Bouman, W.P.1
Pinner, G.2
Johnson, H.3
-
5
-
-
0028939902
-
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
-
Buiting K., Saitoh S., Gross S., Dittrich B., Schwartz S., Nicholls R. D. et al. (1995) Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genetics 9, 395-400.
-
(1995)
Nature Genetics
, vol.9
, pp. 395-400
-
-
Buiting, K.1
Saitoh, S.2
Gross, S.3
Dittrich, B.4
Schwartz, S.5
Nicholls, R.D.6
-
6
-
-
0026595355
-
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 14q11-13
-
Dittrich B., Robinson W. P., Knoblauch H., Buiting H., Schmidt K., Gillessen G. et al. (1992) Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 14q11-13. Human Genetics 90, 313-15.
-
(1992)
Human Genetics
, vol.90
, pp. 313-315
-
-
Dittrich, B.1
Robinson, W.P.2
Knoblauch, H.3
Buiting, H.4
Schmidt, K.5
Gillessen, G.6
-
7
-
-
0027476242
-
Prader-Willi syndrome: Consensus diagnostic criteria
-
Holm V. A., Cassidy S. B., Butler M. G., Hanchett J. M., Greenswag L. R., Whitman B. Y. et al. (1993) Prader-Willi syndrome: Consensus diagnostic criteria. Pediatrics 91, 398-402.
-
(1993)
Pediatrics
, vol.91
, pp. 398-402
-
-
Holm, V.A.1
Cassidy, S.B.2
Butler, M.G.3
Hanchett, J.M.4
Greenswag, L.R.5
Whitman, B.Y.6
-
8
-
-
0031933868
-
Growth hormone treatment of children with Prader-Willi syndrome affects linear growth and body composition favourably
-
Lindgren A-C., Hagenäs L., Müller J., Blichfeldt S., Rosenborg M., Brismar T. et al. (1998) Growth hormone treatment of children with Prader-Willi syndrome affects linear growth and body composition favourably. Acta Paediatrica 87, 28-31.
-
(1998)
Acta Paediatrica
, vol.87
, pp. 28-31
-
-
Lindgren, A.-C.1
Hagenäs, L.2
Müller, J.3
Blichfeldt, S.4
Rosenborg, M.5
Brismar, T.6
-
10
-
-
84874717528
-
-
Prader-Willi Syndrome Publications PWSA (USA), 5700 Midnight Pass Road, Suite 6, Sarasota, Florida 34242
-
Prader-Willi Syndrome. Medical alerts. Prader-Willi Syndrome Publications PWSA (USA), 5700 Midnight Pass Road, Suite 6, Sarasota, Florida 34242. 2004.
-
(2004)
Prader-Willi Syndrome. Medical Alerts
-
-
-
11
-
-
0028229959
-
Imprinting mutations suggested by abnormal DNA methylation pattern in familial Angelman and Prader-Willi syndromes
-
Reis A., Dittrich B., Greger V., Buiting K., Lalande M., Gillessen-Kaesbach G. et al. (1994) Imprinting mutations suggested by abnormal DNA methylation pattern in familial Angelman and Prader-Willi syndromes. American Journal of Human Genetics 54, 741-7.
-
(1994)
American Journal of Human Genetics
, vol.54
, pp. 741-747
-
-
Reis, A.1
Dittrich, B.2
Greger, V.3
Buiting, K.4
Lalande, M.5
Gillessen-Kaesbach, G.6
-
12
-
-
0141516425
-
The syndrome of inappropriate antidiuretic hormone secretion
-
In: 10th edn. (ed. P. Larsen etal.), W. B. Saunders, Philadelphia, PA
-
Robinson A. G. & Verbalis J. G. (2003) The syndrome of inappropriate antidiuretic hormone secretion. In: Textbook of Endocrinology, 10th edn. (ed. P. Larsen etal.), pp. 300-13. W. B. Saunders, Philadelphia, PA.
-
(2003)
Textbook of Endocrinology
, pp. 300-313
-
-
Robinson, A.G.1
Verbalis, J.G.2
-
13
-
-
0031033307
-
Water intoxication in a patient with the Prader-Willi syndrome treated with desmopressin for nocturnal enuresis
-
Robson W. L. M., Shashi V., Nagaraj S. & Norgaard J. P. (1997) Water intoxication in a patient with the Prader-Willi syndrome treated with desmopressin for nocturnal enuresis. The Journal of Urology 157, 646-7.
-
(1997)
The Journal of Urology
, vol.157
, pp. 646-647
-
-
Robson, W.L.M.1
Shashi, V.2
Nagaraj, S.3
Norgaard, J.P.4
-
14
-
-
0028946692
-
Hyponatremia and the syndrome of inappropriate antidiuretic hormone secretion (SIADH) induced by psychotropic drugs
-
Spigset O. & Hedenmalm K. (1995) Hyponatremia and the syndrome of inappropriate antidiuretic hormone secretion (SIADH) induced by psychotropic drugs. Drug Safety 12, 209-25.
-
(1995)
Drug Safety
, vol.12
, pp. 209-225
-
-
Spigset, O.1
Hedenmalm, K.2
-
15
-
-
0031895056
-
Hyponatremia associated with the use of selective serotonin re-uptake inhibitors
-
Strachan J. & Shepherd J. (1998) Hyponatremia associated with the use of selective serotonin re-uptake inhibitors. Australian and New Zealand Journal of Psychiatry 32, 295-8.
-
(1998)
Australian and New Zealand Journal of Psychiatry
, vol.32
, pp. 295-298
-
-
Strachan, J.1
Shepherd, J.2
-
16
-
-
0028852641
-
Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: A study of five cases
-
Swaab D. F., Purba J. S. & Hofman M. A. (1995) Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: A study of five cases. Journal of Clinical Endocrinology and Metabolism 80, 573-9.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 573-579
-
-
Swaab, D.F.1
Purba, J.S.2
Hofman, M.A.3
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