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- Concolino, D
- Piccione, M
- Lo Giudice, C
- Vicari, S
Producer: 20040601
In:
Acta paediatrica (Oslo, Norway : 1992) vol. 92
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Subclinical hypothyroidism and Down's syndrome; studies on myocardial structure and function. [electronic resource] by
- Toscano, E
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- Di Maio, S
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- Del Giudice, E
- Caniello, B
- Calabrò, R
- Andria, G
Producer: 20031211
In:
Archives of disease in childhood vol. 88
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25.
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Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency. [electronic resource] by
- Indo, Y
- Mardy, S
- Miura, Y
- Moosa, A
- Ismail, E A
- Toscano, E
- Andria, G
- Pavone, V
- Brown, D L
- Brooks, A
- Endo, F
- Matsuda, I
Producer: 20020122
In:
Human mutation vol. 18
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Lifetime psychopathology in child and adolescent offspring of parents diagnosed with schizophrenia or bipolar disorder: a 2-year follow-up study. [electronic resource] by
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- Sugranyes, G
- Baeza, I
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- Rodríguez-Toscano, E
- Espliego, A
- Ayora, M
- Romero, S
- Sánchez-Gistau, V
- Castro-Fornieles, J
Producer: 20210315
In:
European child & adolescent psychiatry vol. 30
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28.
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Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor. [electronic resource] by
- Mardy, S
- Miura, Y
- Endo, F
- Matsuda, I
- Sztriha, L
- Frossard, P
- Moosa, A
- Ismail, E A
- Macaya, A
- Andria, G
- Toscano, E
- Gibson, W
- Graham, G E
- Indo, Y
Producer: 19990624
In:
American journal of human genetics vol. 64
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Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive proband. [electronic resource] by
- Xiang, A H
- Azen, S P
- Raffel, L J
- Tan, S
- Cheng, L S
- Diaz, J
- Toscano, E
- Henderson, P C
- Hodis, H N
- Hsueh, W A
- Rotter, J I
- Buchanan, T A
Producer: 20010118
In:
Circulation vol. 103
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30.
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Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive hispanic families. [electronic resource] by
- Cheng, L S
- Davis, R C
- Raffel, L J
- Xiang, A H
- Wang, N
- Quiñones, M
- Wen, P Z
- Toscano, E
- Diaz, J
- Pressman, S
- Henderson, P C
- Azen, S P
- Hsueh, W A
- Buchanan, T A
- Rotter, J I
Producer: 20011011
In:
Circulation vol. 104
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31.
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Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. [electronic resource] by
- Goldberg, Y P
- MacFarlane, J
- MacDonald, M L
- Thompson, J
- Dube, M-P
- Mattice, M
- Fraser, R
- Young, C
- Hossain, S
- Pape, T
- Payne, B
- Radomski, C
- Donaldson, G
- Ives, E
- Cox, J
- Younghusband, H B
- Green, R
- Duff, A
- Boltshauser, E
- Grinspan, G A
- Dimon, J H
- Sibley, B G
- Andria, G
- Toscano, E
- Kerdraon, J
- Bowsher, D
- Pimstone, S N
- Samuels, M E
- Sherrington, R
- Hayden, M R
Producer: 20070621
In:
Clinical genetics vol. 71
Availability: No items available.
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