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10 families with benign familial hematuria. Considerations on prevalence, genetics and clinical and urine characteristics
10 families with benign familial hematuria. Considerations on prevalence, genetics and clinical and urine characteristics
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10 families with benign familial hematuria. Considerations on prevalence, genetics and clinical and urine characteristics

Li Volti, S ; D'Avola, M A ; Mollica, F

Minerva pediatrica, 1989-07, Vol.41 (7), p.367-370

Italy

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2
10-Year outcome of childhood epilepsy in well-functioning children and adolescents
10-Year outcome of childhood epilepsy in well-functioning children and adolescents
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10-Year outcome of childhood epilepsy in well-functioning children and adolescents

Jonsson, Pysse ; Eeg-Olofsson, Orvar

European journal of paediatric neurology, 2011-07, Vol.15 (4), p.331-337 [Periódico revisado por pares]

England: Elsevier Ltd

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3
100 Midlife Women With Eating Disorders: A Phenomenological Analysis of Etiology
100 Midlife Women With Eating Disorders: A Phenomenological Analysis of Etiology
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100 Midlife Women With Eating Disorders: A Phenomenological Analysis of Etiology

Kally, Zina ; Cumella, Edward J.

The Journal of general psychology, 2008-10, Vol.135 (4), p.359-378 [Periódico revisado por pares]

United States: Heldref

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4
104th European Neuromuscular Centre (ENMC) International Workshop: Distal myopathies, 8–10th March 2002 in Naarden, The Netherlands
104th European Neuromuscular Centre (ENMC) International Workshop: Distal myopathies, 8–10th March 2002 in Naarden, The Netherlands
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104th European Neuromuscular Centre (ENMC) International Workshop: Distal myopathies, 8–10th March 2002 in Naarden, The Netherlands

Udd, B ; Bushby, K ; Nonaka, I ; Griggs, R

Neuromuscular disorders : NMD, 2002-11, Vol.12 (9), p.897-904 [Periódico revisado por pares]

England: Elsevier B.V

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5
10th International Conference on Health Education
10th International Conference on Health Education
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10th International Conference on Health Education

Angst, H

Krankenpflege. Soins infirmiers, 1980 (5), p.266-267

Switzerland

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6
11 things you should talk to your doctor about. It's easy to suggest that you talk to your doctor. It's much harder to know what to say
11 things you should talk to your doctor about. It's easy to suggest that you talk to your doctor. It's much harder to know what to say
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11 things you should talk to your doctor about. It's easy to suggest that you talk to your doctor. It's much harder to know what to say

Harvard health letter, 2004-03, Vol.29 (5), p.1-2

United States

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7
12. The genetic counselor as psychotherapist
12. The genetic counselor as psychotherapist
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12. The genetic counselor as psychotherapist

Kessler, S

Birth defects original article series, 1979, Vol.15 (2), p.187

United States

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8
1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis
1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis
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1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis

Nesterova, Galina ; Malicdan, May Christine ; Yasuda, Kaori ; Sakaki, Toshiyuki ; Vilboux, Thierry ; Ciccone, Carla ; Horst, Ronald ; Huang, Yan ; Golas, Gretchen ; Introne, Wendy ; Huizing, Marjan ; Adams, David ; Boerkoel, Cornelius F ; Collins, Michael T ; Gahl, William A

Clinical journal of the American Society of Nephrology, 2013-04, Vol.8 (4), p.649-657 [Periódico revisado por pares]

United States: American Society of Nephrology

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9
13-year period of application of the 13C-urease breath test for determining Helicobacter pylori in Russian clinical practice
13-year period of application of the 13C-urease breath test for determining Helicobacter pylori in Russian clinical practice
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13-year period of application of the 13C-urease breath test for determining Helicobacter pylori in Russian clinical practice

Rapoport, S I ; Shubina, N A

Klinicheskaia meditsina, 2014, Vol.92 (11), p.59 [Periódico revisado por pares]

Russia (Federation)

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10
14q(22) deletion in a familial case of anophthalmia with polydactyly
14q(22) deletion in a familial case of anophthalmia with polydactyly
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14q(22) deletion in a familial case of anophthalmia with polydactyly

Ahmad, M.E. ; Dada, Rima ; Dada, Tanuj ; Kucheria, Kiran

American journal of medical genetics, 2003-07, Vol.120A (1), p.117-122 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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Deste Autor:

  1. Mishima, S
  2. Pereira, M
  3. Matumoto, S
  4. Silva, C
  5. Chiesa, A

Neste Assunto:

  1. Family Health
  2. Family Health
  3. Humans
  4. Science & Technology
  5. Life Sciences & Biomedicine

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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