KL Herbst, LR Tannock, SS Deeb, JQ Purnell, … - Diabetes care, 2003 - Am Diabetes Assoc RESULTS—Only women with clinical features of FPLD1 have been identified.
Although they lack extremity and gluteal subcutaneous fat, they do have truncal
obesity. Skinfold thickness on the arm and leg was significantly less than ... Cited by 23 - Related articles - BL Direct - All 6 versions
- ►diabetesjournals.org WA Haque, EA Oral, K Dietz, AM Bowcock, AK … - Diabetes Care, 2003 - Am Diabetes Assoc RESULTS—We studied 52 women and 24 men with FPLD from 18 different families.
Twenty-eight women (54%) but only four men (17%) had diabetes (P < 0.001);
therefore further comparisons were mostly limited to women. Compared with ... Cited by 21 - Related articles - BL Direct - All 5 versions
- ►endojournals.org V Simha, A Garg - Journal of Clinical Endocrinology & Metabolism, 2002 - Endocrine Soc Mandibuloacral dysplasia (MAD) is a rare autosomal recessive disorder that is
characterized by mandibular and clavicular hypoplasia, acroosteolysis, delayed
closure of cranial sutures, joint contractures, and mottled cutaneous ... Cited by 53 - Related articles - BL Direct - All 6 versions
- ►endojournals.org V Simha, A Garg - Journal of Clinical Endocrinology & Metabolism, 2003 - Endocrine Soc Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive
syndrome characterized by extreme paucity of adipose tissue since birth,
acanthosis nigricans, severe insulin resistance, marked ... Cited by 36 - Related articles - BL Direct - All 4 versions
WA Haque, F Vuitch, A Garg - Diabetic Medicine, 2002 - interscience.wiley.com ResultsPatient 1, a 66-year-old woman with the R482Q mutation, had diabetes
mellitus, dyslipidaemia, and coronary artery disease and died suddenly. Autopsy
confirmed the typical body fat distribution and further revealed excess fat ... Cited by 21 - Related articles - BL Direct - All 4 versions
- ►endojournals.org A Garg - Journal of Clinical Endocrinology & Metabolism, 2000 - Endocrine Soc Familial partial lipodystrophy, Dunnigan type (FPLD; Mendelian Inheritance in
Man #151660), is an autosomal dominant disorder characterized by loss of sc fat
from the extremities and trunk since puberty and predisposition to insulin ... Cited by 65 - Related articles - BL Direct - All 6 versions
- ►endojournals.org AK Agarwal, V Simha, EA Oral, SA Moran, P … - Journal of Clinical Endocrinology & Metabolism, 2003 - Endocrine Soc CONGENITAL GENERALIZED LIPODYSTROPHY [CGL; Berardinelli-Seip syndrome, Online
Mendelian Inheritance in Man (OMIM) no. 269700; http://www.ncbi.nlm.nih.gov/Omim
/] is a rare autosomal recessive disorder characterized by near complete ... Cited by 63 - Related articles - BL Direct - All 5 versions
A Misra, A Garg - Medicine, 2003 - journals.lww.com Abstract: We present clinical descriptions, metabolic features, and patterns of
body fat loss of 16 patients with acquired general- ized lipodystrophy (AGL)
seen by us over the last 10 years. In ad- dition, we review 63 cases of AGL ... Cited by 54 - Related articles - BL Direct - All 4 versions
EK Pivnick, B Angle, RA Kaufman, BD Hall, P … - American journal of medical genetics, 2000 - interscience.wiley.com The neonatal progeroid syndrome (NPS), or Wiedemann-Rautenstrauch, is a rare
autosomal recessive disorder comprised of generalized lipoatrophy except for fat
pads in the suprabuttock areas, hypotrichosis of the scalp hair, eyebrows, ... Cited by 31 - Related articles - BL Direct - All 3 versions
PW Mathieson, K Peters - American journal of kidney diseases, 1994 - cat.inist.fr ARE NEPHRITIC FACTORS NEPHRITOGENIC? PW MATHIESON, K PETERS American journal
of kidney diseases 24:66, 964-966, Elsevier, 1994.
Cited by 10 - Related articles - BL Direct - All 2 versions
