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Теппермен Дж., Теппермен Х. Физиология обмена веществ и эндокринной системы. М.: Мир, 1989. 656 с.
Тиц Н. У. Энциклопедия клинических лабораторных тестов. М.: Лабинформ, 1997. 960 с.
De Grazia J. A., Ivanovich P., Fellows H., Rich C. A double isotope method for measurement of intestinal absorption of calcium in man // Journal of Laboratory and Clinical Medicine. 1965. Vol. 66. P. 822-829.
оабник з неонатологп: Пер. з англ. / Ред. Джон П. Клоерп, Ерш К. Ейхенвальд, ЕннР. Старк. Шосте видання. К.: Фонд допомоги i розвитку датям Чорнобиля; Вид-во «Фешкс», 2010. 856 с.
Sulaiman R. A., Sharratt C. L., Lee P. W. et al. Ethnic differences in umbilical cord blood vitamin D and parathyroid hormone — South Asians compared to Whites born in the UK // J. Matern. Fetal Neonatal. Med. 2010. Vol. 23, N 11. P. 1315-1317.
Шабалов Н. П. ред. Неонатология: учеб. пособие: в 2 т. 5-е изд., испр. и доп. М.: МЕДпресс-информ, 2009.
Берман Р. Э., Клигман Р. М., Дженсон Х. Б. Педиатрия по Нельсону в пяти томах: руководство: пер. с англ. М.: Рид Элсивер, 2009.
Kayem G., Bernier-Dupreelle A., Goffinet F. et al. Active versus expectant management for preterm prelabor rupture of membranes at 34-36 weeks of completed gestation: comparison of maternal and neonatal outcomes // Acta Obstet. Gynecol. Scand. 2010. Vol. 89, N 6. P. 776-781.
Betti M., Ceccatelli G., Belcari F. et al. Neonatal outcome in newborns from mothers with endocrinopathies // Gynecol. Endocrinol. 2011. Vol. 27, N 4. P. 248-250.
Hay W. W. Jr. Care of the infant of the diabetic mother // Curr Diab ReP. 2012. Vol 12, N 1. P. 4-15.
MitanchezD. Foetal and neonatal complications in gestational diabetes: perinatal mortality, congenital malformations, macrosomia, shoulder dystocia, birth injuries, neonatal complications // Diabetes Metab. 2010. Vol. 36, N 6, Pt. 2. P. 617-27.
Зилва Дж. Ф., Пэннел П. Р. Клиническая химия в диагностике и лечении. М.: Медицина, 1988. 528 с.
Tsao P. C., Chang F. Y., Chen S. J. et al. Sudden and unexpected and near death during the early neonatal period: a multicenter study // J. Chin. Med. Assoc. 2012. Vol. 75, N 2. P. 65-69.
Иванов Д. О. Клинико-лабораторные варианты течения сепсиса новорожденных: Автореф. дис... док. мед. наук. СПб., 2002.
Жидкова О. Н. Взаимосвязь уровней электролитов крови с функциональным состоянием сердечной мышцы у детей, родившихся в асфиксии, в раннем неонатальном периоде: Автореф. дис... канд. мед. наук. СПб., 1998.
Hillman L. S., Rojanasathit S., Slatopolsky E., Haddad J. G. Serial measurements of serum calcium, magnesium, parathyroid hormone, calcitonin, and 25-hydroxy-vitamin D in premature and term infants during the first week of life // Pediatr Res. 1977. Vol. 11, N 6. P. 739-744.
Guran T., Akcay T., Bereket A. et al. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes //Nephrol Dial Transplant. 2012. Vol. 27. P. 667
Malloy P. J., Wang J., Srivastava T., Feldman D. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor // Mol. Genet. Metab. 2010. Vol. 99, N 1. P. 72.
Nakajima K., Yamazaki K., Kimura H. et al. Novel gain of function mutations of the calcium-sensing receptor in two patients with PTH-deficient hypocalcemia // Intern. Med. 2009. Vol. 48, N 22. P. 19511956.
Bui T., Christin-Maitre S. [Vitamin D and pregnancy] // Ann. Endocrinol. (Paris). 2011. Vol. 72, Suppl 1. P. S23-S28.
Barrett H., McElduff A. Vitamin D and pregnancy: An old problem revisited // Best. Pract. Res. Clin. Endocrinol. Metab. 2010. Vol. 24, N 4. P. 527-539.
Stathopoulos I. P., Liakou C. G., Katsalira A. et al. The use of bisphosphonates in women prior to or during pregnancy and lactation // Hormones (Athens). 2011. Vol. 10, N 4. P. 280-291.
Panzaru M., Rusu C., Volosciuc M. et al. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome] // Rev. Med. Chir. Soc. Med. Nat. Iasi. 2011. Vol. 115, N 3. P. 756-761.
Molesky M. G. Chromosome 22q11.2 microdeletion syndrome. // Neonatal. Netw. 2011. Vol. 30, N 5. P. 304-311.
Patra S., Singh V., Pemde H. K, Chandra J. Case series of neonatal hypocalcemia due to pseudohypoparathyroidism // J. Pediatr. Endocrinol. Metab. 2010. Vol. 23, N 10. P. 1073-1075.
de Arriba Munoz A., Labarta Aizpun J. I., Dehesa E. M. et al. [Different expression of the Asn264LysfsX35 mutation of the GNAS gene in a family with pseudohypoparathyroidism] //An. Pediatr. (Barc). 2011. Vol. 74, N 2. P. 116-121.
Naguib K. K, Gouda S. A, Elshafey A. et al. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait // East. Mediterr. Health. J. 2009. Vol. 15, N 2. P. 345-352.
Stark Z., Savarirayan R.. Osteopetrosis // Orphanet J Rare Dis. 2009. Vol. 20, N 4. P. 5.
Engiz O., Kara S., Bagrul D. et al. Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia // J. Pediatr. Endocrinol. Metab. 2012. Vol. 25, N 11-12. P. 1205-1207.
David L., Anast C. S. Calcium metabolism in newborn infants: The interrelationship of parathyroid function and calcium, magnesium, and phosphorus metabolism in normal, “sick,” and hypocalcemic newborns // J. Clin. Invest. 1974. Vol. 54. P. 287-296.
David L., Salle B. L., Putet G., Grafmeyer D. C. Serum immunoreactive calcitonin in low birth weight infants. Description of early changes; effect of intravenous calcium infusion; relationships with early changes in serum calcium, phosphorus, magnesium, parathyroid hormone, and gastrin levels // Pediatr. Res. 1981. Vol. 15. P. 803.
Glorieux F., Salle B. L., Delvin E. et al. Vitamin D metabolism in preterm infants: serum calcitriol values during the first five days of life // J. Pediatr. 1981. Vol. 99. P. 640-644.
Czech-Kowalska J., Pludowski P., Dobrzanska A., Kryskiewicz E., Karczmarewicz E., Gruszfeld D., Pleskaczynska A., GolkowskaM. Impact of vitamin D supplementation on markers of bone mineral metabolism in term infants // Bone. 2012. Vol. 51 (4). P. 781-786.
LaziC-Mitrovic T., Djukic M., Cutura N. et al. [Transitory hypothermia as early prognostic factor in term newborns with intrauterine growth retardation] // SrP. Arh. Celok. Lek. 2010. Vol. 138 (9-10). P. 604-608.
Шабалов Н. П. ред. Неонатология: Учебное пособие в 2 т. Т. I. М.: МЕДпресс-информ, 2004. 640 с.
Mehrotra P., Marwaha R. K., Aneja S. et al. Hypovitaminosis d and hypocalcemic seizures in infancy // Indian Pediatr. 2010. Vol. 47, N 7. P. 581-586.
Папаян А.В., Стяжкина И.С. Неонатальная нефрология. Руководство. СПб, Питер. 2002. 185 с
Sloan S. R. Neonatal transfusion review // Paediatr Anaesth. 2011. Vol. 21, N 1. P. 25-30.
Hosseinpour Sakha S., Gharehbaghi M. M. Exchange transfusion in severe hyperbilirubinemia: an experience in northwest Iran // Turk. J. Pediatr. 2010. Vol. 52, N 4. P. 367-371.
Ladenhauf H. N., Stundner O., Spreitzhofer F., et al. Severe hyperphosphatemia after administration of sodium-phosphate containing laxatives in children: case series and systematic review of literature // Pediatr. Surg. Int. 2012. Vol. 28, N 8. P. 805-814.
Al Azkawi H., Al Mutair A. Newborn with dilated cardiomyopathy secondary to vitamin D deficiency // Case Rep Pediatr. 2012. URL: http://www.hindawi.com/crim/pediatrics/2012/945437/cta/ (дата доступа: 25.02.2013).
Лисс В. Л., Нагорная И. И., Николаева Л. В., Плотникова Е. В., Скородок Ю. Л., Пальчик А. Б., Шабалов Н. П. Диагностика и лечение эндокринных заболеваний у детей и подростков: Справочник/ Под ред. проф. Н. П. Шабалова. М.: МЕДпресс-информ, 2003. 544 с.
Mihatsch W., Trotter A., Pohlandt F. Calcium and phosphor intake in preterm infants: sensitivity and specifity of 6-hour urine samples to detect deficiency // Klin. Padiatr. 2012. Vol. 224, N 2. P. 61-65.
Секреты неонатологии и перинатологии. Полин Ричард А., Спитцер АланР. М.: Бином, 2011. 624 С.
Chen T. K., Yang C. Y., Chen S. J. Calcinosis cutis complicated by compartment syndrome following extravasation of calcium gluconate in a neonate: a case report // Pediatr. Neonatol. 2010. Vol. 51, N 4. P. 238-241.
Неонатология / под ред. Т. Л. Гомеллы, М. Д. Каннигам. М.: Медицина, 1995. 640 с.
Young T. E., Magnum B. Neofax: A Manual of drugs used in neonatal care, ed 13. Raleigh, North Carolina: Acorn Publishing, USA, 2000. P. 195-197.
48. Бауман В. К. Всасывание двухвалентных катионов // Физиология всасывания / под ред. В. К. Бауман. Л.: Наука, 1977. C. 152-222.
Mitchell D. M., Juppner H. Regulation of calcium homeostasis and bone metabolism in the fetus and neonate // Curr Opin Endocrinol Diabetes Obes. 2010. Vol. 17, N 1. P. 25-30.
Raue F., Pichl J., Dorr H. G. et al. Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia — a German survey // Clin. Endocrinol. (Oxf). 2011. Vol. 75, N 6. P. 760-765.
Bayindir P., Guillerman R. P., Hicks M. J., Chintagumpala M. M. Cellular mesoblastic nephroma (infantile renal fibrosarcoma): institutional review of the clinical, diagnostic imaging, and pathologic features of a distinctive neoplasm of infancy // Pediatr. Radiol. 2009. Vol. 39, N 10.P. 1066-1074.
Nesargi S. V., Bhat S. R., Rao H. N. S. et al. Hypercalcemia in extremely low birth weight neonates // Indian. J. Pediatr. 2012. Vol. 79, N 1. P. 124-126.
Ichikawa G., Watabe Y., Suzumura H. et al. Hypophosphatemia in small for gestational age extremely low birth weight infants receiving parenteral nutrition in the first week after birth // J. Pediatr. Endocrinol. Metab. 2012. Vol. 25, N 3-4. P. 317-321.
Wilhelm-Bals A., Parvex P., Magdelaine C., GirardinE. Successful use of bisphosphonate and calcimimetic in neonatal severe primary hyperparathyroidism // Pediatrics. 2012. Vol. 129, N 3. P. e812-e816.
Al-Shanafey S., Al-Hosaini R., Al-Ashwal A., Al-RabeeahA. Surgical management of severe neonatal hyperparathyroidism: one center’s experience // J. Pediatr. Surg. 2010. Vol. 45, N 4. P. 714-717.
Al-Khalaf F. A., Ismail A., Soliman A. T. et al. Neonatal severe hyperparathyroidism: further clinical and molecular delineation // Eur. J. Pediatr. 2011. Vol. 170, N 5. P. 625-631.
Paul R. G., Elston M. S., Gill A. J. et al. Hypercalcaemia due to parathyroid carcinoma presenting in the third trimester of pregnancy // Aust. N. Z. J. Obstet. Gynaecol. 2012. Vol. 52, N 2. P. 204-207.
Varghese J, Rich T, Jimenez C. Benign familial hypocalciuric hypercalcemia. Endocr Pract. 2011. Vol. 17, Suppl 1. P. 13-7.
Rodrigues L. S., Cau A. C., Bussmann L. Z. et al. New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) // Arq. Bras. Endocrinol. Metabol. 2011. Vol. 55, N 1. P. 67-71.
Jack M. M., Stone M. L., Clifton-Bligh R. Neonatal hypercalcemia due to polymorphisms of the calcium sensing receptor // J. Pediatr. Endocrinol. Metab. 2009. Vol. 22, N 6. P. 561-563.
McMullen T. P., Learoyd D. L., Williams D. C. et al. Hyperparathyroidism in pregnancy: options for localization and surgical therapy // World. J. Surg. 2010. Vol. 34. P. 1811-1816.
Cetinkaya R., Uyanik A., Keles M., Bilen Y. The rhabdomyolysis related acute renal failure and biphasic calcium metabolism // Pak. J. Med. Sci. 2009. Vol. 25, N 1. P. 152-154.
Srivastava T., Kats A., Martin T. J. et al. Parathyroid-hormone-related protein-mediated hypercalcemia in benign congenital mesoblastic nephroma // Pediatr. Nephrol. 2011. Vol. 26, N 5. P. 799-803.
Czosek R. J., Berul C. I. Congenital long-QT syndrome concealed by hypercalcemia in Williams Syndrome // J. Cardiovasc. Electrophysiol. 2008. Vol. 19, N 12. P. 1322-1324.
Komoike Y., Fujii K., Nishimura A. et al. Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly // Genesis. 2010. Vol. 48, N 4. P. 233-243.
Oliveira A. C., Selores M., Pereira O. Fat necrosis of the newborn — report on two cases // An Bras Dermatol. 2011. Vol. 86, N 4, Suppl. 1. P. S114-S117.
Savic D. M., Stojanovic N. D., Stankovic V. D. et al. Subcutaneous fat necrosis in newborns //Med. Glas. (Zenica). 2012. Vol. 9, N 2. P. 429-431.
Hogeling M., Meddles K., Berk D. R. et al. Extensive subcutaneous fat necrosis of the newborn associated with therapeutic hypothermia // Pediatr. Dermatol. 2012. Vol. 29. P. 59-63.
Akcay A., Akar M., Oncel M. Y. et al. Hypercalcemia due to subcutaneous fat necrosis in a newborn after total body cooling // Pediatr. Dermatol. 2013. Vol. 30, N 1. P. 120-123.
Alaoui K., Abourazzak S., Oulmaati A. et al. An unusual complication of subcutaneous fat necrosis of the newborn // BMJ Case ReP. 2011. URL: http://www.ncbi.nlm.nih.gov/pubmed/22696743 (дата доступа: 25.02.2013).
Akin M. A., Akin L., Coban D. et al. Post-operative subcutaneous fat necrosis in a newborn: a case report // Fetal. Pediatr. Pathol. 2011. Vol. 30, N 6. P. 363-369.
Eller-Vainicher C., Chiodini I., Battista C. et al. Sporadic and MEN1-related primary hyperparathyroidism: differences in clinical expression and severity // J. Bone. Miner. Res. 2009. Vol. 24, N 8. P. 1404-1410.
Vanstone M. B., Oberfield S. E., Shader L. et al. Hypercalcemia in children receiving pharmacologic doses of vitamin D // Pediatrics. 2012. Vol. 129, N 4. P. e1060-3.
Nguyen M., Boutignon H., Mallet E. et al. Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment // J. Pediatr. 2010. Vol. 157. P. 296-302.
Gatti D., Viapiana O., Idolazzi L. et al. Neridronic acid for the treatment of bone metabolic diseases // Expert. Opin. Drug. Metab. Toxicol. 2009. Vol. 5, N 10. P. 1305-1311.
Koltin D., Rachmiel M., Wong B. Y. et al. Mild infantile hypercalcemia: diagnostic tests and outcomes // J. Pediatr. 2011. Vol. 159, N 2. P. 215-221.

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